Variant report

Variant	nsv872460
Chromosome Location	chr1:155151493-155163181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:855)
Chromatin interactive
region (count:74)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155163135-155163500	K562	blood:	n/a	n/a
2	ATF2	chr1:155163180-155163620	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:155163143-155163855	A549	lung:	n/a	chr1:155163657-155163677
4	BACH1	chr1:155163141-155163800	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:155158577-155158581	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr1:155157852-155158151	GM12878	blood:	n/a	n/a
7	BCL3	chr1:155162937-155164820	A549	lung:	n/a	n/a
8	BCL3	chr1:155163030-155163766	A549	lung:	n/a	n/a
9	BCL3	chr1:155157821-155158153	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:155163064-155164834	K562	blood:	n/a	n/a
11	BHLHE40	chr1:155157785-155158391	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:155161078-155161718	HepG2	liver:	n/a	n/a
13	BRCA1	chr1:155162848-155163722	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:155163005-155163071	GM12878	blood:	n/a	n/a
15	CBX3	chr1:155162734-155164889	K562	blood:	n/a	n/a
16	CCNT2	chr1:155162883-155163703	K562	blood:	n/a	chr1:155162948-155162957 chr1:155162941-155162950
17	CEBPB	chr1:155162858-155163005	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:155151321-155151701	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:155151261-155151798	MCF-7	breast:	n/a	n/a
20	CEBPB	chr1:155151384-155151663	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:155151317-155151671	K562	blood:	n/a	n/a
22	CEBPB	chr1:155151303-155151743	K562	blood:	n/a	n/a
23	CEBPB	chr1:155151325-155151674	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:155151314-155151701	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:155151241-155151779	A549	lung:	n/a	n/a
26	CEBPB	chr1:155151315-155151708	A549	lung:	n/a	n/a
27	CEBPB	chr1:155151394-155151709	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr1:155151254-155151748	K562	blood:	n/a	n/a
29	CEBPB	chr1:155151312-155151692	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:155151307-155151705	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr1:155151319-155151676	A549	lung:	n/a	n/a
32	CEBPB	chr1:155151336-155151600	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:155151256-155151770	HepG2	liver:	n/a	n/a
34	CEBPD	chr1:155151249-155151680	HepG2	liver:	n/a	n/a
35	CEBPD	chr1:155151375-155151630	HepG2	liver:	n/a	n/a
36	CEBPD	chr1:155151244-155151761	K562	blood:	n/a	n/a
37	CHD1	chr1:155163111-155163736	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438
38	CHD2	chr1:155162779-155163841	Hela-S3	cervix:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
39	CHD2	chr1:155162771-155163764	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
40	CHD2	chr1:155162872-155163732	GM12878	blood:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
41	CHD2	chr1:155157486-155158278	GM12878	blood:	n/a	n/a
42	CHD2	chr1:155162681-155163821	K562	blood:	n/a	chr1:155162743-155162753 chr1:155163428-155163438 chr1:155162947-155162957
43	CREB1	chr1:155162981-155163810	A549	lung:	n/a	n/a
44	CTBP2	chr1:155162860-155163792	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:155158120-155158270	HRE	kidney:	n/a	n/a
46	CTCF	chr1:155158091-155158148	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:155158070-155158222	GM19240	blood:	n/a	n/a
48	CTCF	chr1:155158040-155158190	GM12865	blood:	n/a	n/a
49	CTCF	chr1:155162782-155163981	A549	lung:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
50	CTCF	chr1:155158020-155158170	HUVEC	blood vessel:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155162756-155162806	T-47D	breast:	n/a
2	chr1:155162756-155162806	T-47D	breast:	n/a
3	chr1:155162756-155162806	ECC-1	luminal epithelium:	n/a
4	chr1:155156300-155156350	HRE	kidney:	n/a
5	chr1:155163013-155163063	NB4	blood:	n/a
6	chr1:155158319-155158369	RPTEC	kidney:	n/a
7	chr1:155163013-155163063	NHBE	bronchial:	n/a
8	chr1:155161221-155161271	Caco-2	colon:	n/a
9	chr1:155162752-155162802	MCF-7	breast:	n/a
10	chr1:155162752-155162802	AG10803	skin:	n/a
11	chr1:155161679-155161729	HCF	heart:	n/a
12	chr1:155162752-155162802	HNPCEpiC	eye:	n/a
13	chr1:155161679-155161729	SKMC	muscle:	n/a
14	chr1:155161833-155161883	AG09319	gingival:	n/a
15	chr1:155161161-155161211	HNPCEpiC	eye:	n/a
16	chr1:155161161-155161211	HCT-116	colon:	n/a
17	chr1:155156300-155156350	HAEpiC	amniotic membrane:	n/a
18	chr1:155161211-155161261	ovcar-3	ovarian:	n/a
19	chr1:155157194-155157244	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:155161784-155161834	PANC-1	pancreas:	n/a
21	chr1:155162752-155162802	GM06990	blood:	n/a
22	chr1:155161784-155161834	Caco-2	colon:	n/a
23	chr1:155161679-155161729	AG04450	lung:	fetal
24	chr1:155161679-155161729	GM19239	blood:	n/a
25	chr1:155163013-155163063	AG09309	skin:	n/a
26	chr1:155156300-155156350	A549	lung:	n/a
27	chr1:155163013-155163063	HepG2	liver:	n/a
28	chr1:155161221-155161271	HRE	kidney:	n/a
29	chr1:155161679-155161729	HL-60	blood:	n/a
30	chr1:155161221-155161271	HepG2	liver:	n/a
31	chr1:155158319-155158369	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:155162752-155162802	HIPEpiC	eye:	n/a
33	chr1:155161784-155161834	GM19239	blood:	n/a
34	chr1:155161784-155161834	HRE	kidney:	n/a
35	chr1:155161833-155161883	ProgFib	skin:	n/a
36	chr1:155157194-155157244	U87	brain:	n/a
37	chr1:155152367-155152417	AG09309	skin:	n/a
38	chr1:155163013-155163063	NH-A	brain:	n/a
39	chr1:155161161-155161211	HCF	heart:	n/a
40	chr1:155162871-155162921	T-47D	breast:	n/a
41	chr1:155161833-155161883	LNCaP	prostate:	n/a
42	chr1:155162752-155162802	CMK	blood:	n/a
43	chr1:155156300-155156350	BE2_C	brain:	n/a
44	chr1:155161221-155161271	H1-hESC	embryonic stem cell:	embryo
45	chr1:155161679-155161729	ProgFib	skin:	n/a
46	chr1:155163013-155163063	RPTEC	kidney:	n/a
47	chr1:155161679-155161729	NHDF-neo	bronchial:	n/a
48	chr1:155161679-155161729	LNCaP	prostate:	n/a
49	chr1:155157194-155157244	ProgFib	skin:	n/a
50	chr1:155157194-155157244	HIPEpiC	eye:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
2	chr1:155162882..155163515-chr8:48873266..48874033,2	Hela-S3	cervix:
3	chr1:155110723..155112742-chr1:155150988..155153173,2	K562	blood:
4	chr1:155162888..155163772-chr1:155196595..155197463,2	MCF-7	breast:
5	chr1:155163154..155164052-chr12:13044571..13045233,2	Hela-S3	cervix:
6	chr1:155106788..155108939-chr1:155162594..155164354,3	MCF-7	breast:
7	chr1:155055270..155058458-chr1:155162731..155164725,3	MCF-7	breast:
8	chr1:155090194..155092132-chr1:155163035..155164929,2	MCF-7	breast:
9	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
10	chr1:155110723..155114225-chr1:155147854..155154401,7	K562	blood:
11	chr1:155162793..155163414-chr17:67323501..67324001,2	Hela-S3	cervix:
12	chr1:155162487..155164653-chr1:155579583..155581273,2	K562	blood:
13	chr1:155105664..155110180-chr1:155143584..155151850,15	MCF-7	breast:
14	chr1:155160293..155162117-chr1:155291803..155294447,2	K562	blood:
15	chr1:155162843..155163672-chr19:47776511..47777264,2	Hela-S3	cervix:
16	chr1:155148758..155149726-chr1:155162834..155163883,7	K562	blood:
17	chr1:155162847..155164513-chr1:155220020..155222402,2	K562	blood:
18	chr1:155149492..155150044-chr1:155161179..155161836,3	MCF-7	breast:
19	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
20	chr1:155163173..155164182-chr10:74032582..74033760,3	Hela-S3	cervix:
21	chr1:155163169..155163906-chr1:155176359..155177228,4	MCF-7	breast:
22	chr1:155161998..155167332-chr1:155208163..155212538,6	K562	blood:
23	chr1:154943189..154945318-chr1:155161226..155163403,2	K562	blood:
24	chr1:155162741..155164778-chr1:155231161..155233767,3	K562	blood:
25	chr1:155162750..155164739-chr1:155293098..155295016,2	MCF-7	breast:
26	chr1:154944711..154947532-chr1:155161851..155164798,3	MCF-7	breast:
27	chr1:155052798..155059451-chr1:155162483..155166744,9	K562	blood:
28	chr1:155162671..155164140-chr15:65588192..65588839,3	Hela-S3	cervix:
29	chr1:155162983..155163857-chr1:155292790..155293293,2	K562	blood:
30	chr1:155163130..155164699-chr1:155531249..155533264,2	K562	blood:
31	chr1:155105295..155110704-chr1:155161873..155165835,7	K562	blood:
32	chr1:154974390..154976020-chr1:155161759..155163515,2	MCF-7	breast:
33	chr1:154945649..154947897-chr1:155163027..155164595,2	K562	blood:
34	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
35	chr1:155162819..155165123-chr1:155223142..155225278,3	K562	blood:
36	chr1:155143901..155153030-chr1:155191166..155199183,23	MCF-7	breast:
37	chr1:155062500..155064343-chr1:155162863..155164814,2	K562	blood:
38	chr1:155148301..155150189-chr1:155162933..155164249,12	MCF-7	breast:
39	chr1:155161177..155163523-chr1:155219674..155222613,2	K562	blood:
40	chr1:155149492..155150014-chr1:155161259..155161836,2	MCF-7	breast:
41	chr1:155162165..155164633-chr1:155276991..155278874,2	K562	blood:
42	chr1:155163009..155163576-chr5:43121348..43122173,2	Hela-S3	cervix:
43	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
44	chr1:155162933..155163891-chr7:150777812..150778399,2	HCT-116	colon:
45	chr1:155161236..155164985-chr1:155290580..155295192,7	K562	blood:
46	chr1:154192824..154194792-chr1:155163140..155164963,2	K562	blood:
47	chr1:155139118..155143025-chr1:155155964..155158470,4	MCF-7	breast:
48	chr1:155145302..155146232-chr1:155163021..155163628,3	K562	blood:
49	chr1:155162899..155163747-chr11:65625244..65625902,2	Hela-S3	cervix:
50	chr1:155163092..155163669-chr12:52445473..52446435,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTCAP2-2	chr1:155162578-155162707	NONHSAT006698
2	lnc-KRTCAP2-2	chr1:155162577-155162700	NONHSAT006696
3	lnc-KRTCAP2-2	chr1:155161654-155162101	NONHSAT006696
4	lnc-KRTCAP2-2	chr1:155161994-155162065	NONHSAT006698

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MUC1	hsa-miR-145-5p	chr1:155158330-155158348

Variant related genes	Relation type
MIR92B	TF binding region
ENSG00000231064	TF binding region
MUC1	TF binding region
ENSG00000273088	TF binding region
MIR92B	CpG island
ENSG00000231064	CpG island
MUC1	CpG island
ENSG00000273088	CpG island
ENSG00000013588	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000143569	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000164896	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000137259	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000068308	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000179085	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000011275	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000202027	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000125459	chromatin interactions

Extended variants
information (count: 525 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11264341	chr1:155151493-155151494	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs569052904	chr1:155151498-155151499	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs374322169	chr1:155151515-155151516	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs148274827	chr1:155151553-155151554	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs559601020	chr1:155151596-155151597	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs533048623	chr1:155151656-155151657	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs368250505	chr1:155151683-155151684	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs551177008	chr1:155151717-155151718	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs569498355	chr1:155151723-155151724	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs9426886	chr1:155151754-155151755	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs549062825	chr1:155151762-155151763	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs567363903	chr1:155151769-155151770	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs375203674	chr1:155151800-155151801	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs553047970	chr1:155151819-155151820	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs534071833	chr1:155151833-155151834	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs114525519	chr1:155151837-155151838	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs570765420	chr1:155151889-155151890	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538932642	chr1:155151891-155151892	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs557624257	chr1:155151892-155151893	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs539806550	chr1:155151911-155151912	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556539810	chr1:155151951-155151952	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543580709	chr1:155151977-155151978	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555508703	chr1:155151989-155151990	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150200936	chr1:155152045-155152046	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570027349	chr1:155152064-155152065	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376438576	chr1:155152084-155152085	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs367820042	chr1:155152093-155152094	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs200248319	chr1:155152094-155152095	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs143047790	chr1:155152120-155152121	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs541041708	chr1:155152124-155152125	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76872124	chr1:155152205-155152206	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs369568615	chr1:155152209-155152210	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372905417	chr1:155152210-155152211	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200280987	chr1:155152212-155152213	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376153941	chr1:155152221-155152222	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201782832	chr1:155152229-155152230	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370747351	chr1:155152239-155152240	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374448627	chr1:155152257-155152258	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144348158	chr1:155152258-155152259	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200642219	chr1:155152266-155152267	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376526448	chr1:155152267-155152268	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs202106443	chr1:155152273-155152274	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs370196346	chr1:155152296-155152297	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563190780	chr1:155152336-155152337	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs148757333	chr1:155152364-155152365	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374432261	chr1:155152368-155152369	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540479338	chr1:155152400-155152401	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139756484	chr1:155152403-155152404	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555672350	chr1:155152455-155152456	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs528552235	chr1:155152474-155152475	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155146400-155157600	Weak transcription	Right Atrium	heart
2	chr1:155146600-155163000	Weak transcription	Aorta	Aorta
3	chr1:155147600-155151600	Weak transcription	Osteobl	bone
4	chr1:155147600-155157200	Weak transcription	Right Ventricle	heart
5	chr1:155148400-155157800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr1:155148800-155154800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:155148800-155155200	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:155149000-155152600	Enhancers	Stomach Mucosa	stomach
9	chr1:155149000-155155400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:155149200-155152200	Enhancers	Placenta	Placenta
11	chr1:155149200-155152800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr1:155149400-155153000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:155149400-155157400	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr1:155149600-155152600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:155149600-155152600	Strong transcription	Primary hematopoietic stem cells	blood
16	chr1:155149600-155152600	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr1:155149600-155152600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:155149600-155152600	Strong transcription	NHLF	lung
19	chr1:155149600-155152800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:155149600-155152800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:155149600-155152800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:155149600-155152800	Strong transcription	Primary T cells from cord blood	blood
23	chr1:155149600-155153200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:155149600-155155000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:155149600-155156600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:155149600-155156800	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr1:155149600-155157400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:155149600-155157400	Weak transcription	Fetal Intestine Large	intestine
29	chr1:155149600-155158000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:155149600-155158200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:155149600-155158800	Weak transcription	A549	lung
32	chr1:155149600-155162000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr1:155149600-155162600	Weak transcription	Small Intestine	intestine
34	chr1:155149600-155162800	Weak transcription	NHDF-Ad	bronchial
35	chr1:155149800-155151600	Weak transcription	Colonic Mucosa	Colon
36	chr1:155149800-155151800	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr1:155149800-155152600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:155149800-155152600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:155149800-155152600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr1:155149800-155152600	Strong transcription	Brain Substantia Nigra	brain
41	chr1:155149800-155152800	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr1:155149800-155152800	Strong transcription	Brain Hippocampus Middle	brain
43	chr1:155149800-155152800	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr1:155149800-155152800	Strong transcription	Fetal Thymus	thymus
45	chr1:155149800-155153000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:155149800-155153000	Strong transcription	Thymus	Thymus
47	chr1:155149800-155153400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr1:155149800-155154200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:155149800-155154400	Weak transcription	Fetal Intestine Small	intestine
50	chr1:155149800-155154400	Weak transcription	Lung	lung

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