Variant report

Variant	nsv1006223
Chromosome Location	chr4:69217756-69540013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2309)
CpG islands
(count:1100)
Chromatin interactive
region (count:58)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2309 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69241809-69241916	K562	blood:	n/a	n/a
2	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:69241724-69242046	HepG2	liver:	n/a	n/a
10	ATF1	chr4:69226955-69227269	K562	blood:	n/a	n/a
11	ATF2	chr4:69275508-69277104	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:69269850-69270608	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:69271370-69272360	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:69273374-69273928	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:69269806-69270384	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:69272567-69273233	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:69271320-69273979	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr4:69274713-69275097	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr4:69274062-69274402	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
22	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
23	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
24	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
25	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
26	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
27	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
28	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:69233545-69233815	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr4:69233648-69233855	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr4:69273602-69273847	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:69275877-69276040	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
36	BHLHE40	chr4:69250331-69250703	K562	blood:	n/a	n/a
37	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
40	BHLHE40	chr4:69241727-69241977	K562	blood:	n/a	n/a
41	BHLHE40	chr4:69226696-69227246	K562	blood:	n/a	n/a
42	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:69249117-69249120	K562	blood:	n/a	n/a
44	BHLHE40	chr4:69241744-69242010	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:69241718-69241986	HepG2	liver:	n/a	n/a
46	BHLHE40	chr4:69226735-69227270	HepG2	liver:	n/a	n/a
47	BRCA1	chr4:69233556-69233810	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr4:69272255-69272927	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr4:69227012-69227512	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr4:69234386-69235223	Hela-S3	cervix:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69381368-69381418	ProgFib	skin:	n/a
2	chr4:69239481-69239531	HIPEpiC	eye:	n/a
3	chr4:69381368-69381418	ProgFib	skin:	n/a
4	chr4:69239481-69239531	HIPEpiC	eye:	n/a
5	chr4:69381368-69381418	HRCEpiC	kidney:	n/a
6	chr4:69312514-69312564	SKMC	muscle:	n/a
7	chr4:69434475-69434525	LNCaP	prostate:	n/a
8	chr4:69522639-69522689	SK-N-SH	brain:	n/a
9	chr4:69218719-69218769	MCF-7	breast:	n/a
10	chr4:69537806-69537856	GM12892	blood:	n/a
11	chr4:69340916-69340966	HEEpiC	esophagus:	n/a
12	chr4:69537826-69537876	HEK293	kidney:	embryo
13	chr4:69434475-69434525	HL-60	blood:	n/a
14	chr4:69514031-69514081	U87	brain:	n/a
15	chr4:69313197-69313247	ECC-1	luminal epithelium:	n/a
16	chr4:69239481-69239531	HCT-116	colon:	n/a
17	chr4:69537806-69537856	HepG2	liver:	n/a
18	chr4:69514031-69514081	LNCaP	prostate:	n/a
19	chr4:69313197-69313247	H1-hESC	embryonic stem cell:	embryo
20	chr4:69434475-69434525	U87	brain:	n/a
21	chr4:69434475-69434525	SK-N-MC	brain:	n/a
22	chr4:69239481-69239531	HEEpiC	esophagus:	n/a
23	chr4:69239481-69239531	HEK293	kidney:	embryo
24	chr4:69435601-69435651	AG10803	skin:	n/a
25	chr4:69312104-69312154	HNPCEpiC	eye:	n/a
26	chr4:69522639-69522689	Jurkat	blood:	n/a
27	chr4:69537826-69537876	A549	lung:	n/a
28	chr4:69536319-69536369	HIPEpiC	eye:	n/a
29	chr4:69340916-69340966	HNPCEpiC	eye:	n/a
30	chr4:69537806-69537856	HIPEpiC	eye:	n/a
31	chr4:69435593-69435643	ProgFib	skin:	n/a
32	chr4:69435593-69435643	HIPEpiC	eye:	n/a
33	chr4:69522639-69522689	Hela-S3	cervix:	n/a
34	chr4:69355121-69355171	GM12878	blood:	n/a
35	chr4:69536319-69536369	PANC-1	pancreas:	n/a
36	chr4:69537806-69537856	NHDF-neo	bronchial:	n/a
37	chr4:69434475-69434525	HAEpiC	amniotic membrane:	n/a
38	chr4:69239481-69239531	LNCaP	prostate:	n/a
39	chr4:69537806-69537856	SKMC	muscle:	n/a
40	chr4:69522639-69522689	PFSK-1	brain:	n/a
41	chr4:69434475-69434525	AG10803	skin:	n/a
42	chr4:69312104-69312154	HRE	kidney:	n/a
43	chr4:69537826-69537876	HCM	heart:	n/a
44	chr4:69434475-69434525	ECC-1	luminal epithelium:	n/a
45	chr4:69381368-69381418	LNCaP	prostate:	n/a
46	chr4:69435250-69435300	Caco-2	colon:	n/a
47	chr4:69218719-69218769	K562	blood:	n/a
48	chr4:69536319-69536369	RPTEC	kidney:	n/a
49	chr4:69381368-69381418	HCM	heart:	n/a
50	chr4:69434475-69434525	HMEC	breast:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:69194867..69197488-chr4:69233410..69236002,2	MCF-7	breast:
2	chr4:69208163..69209683-chr4:69233967..69235522,2	MCF-7	breast:
3	chr4:69215623..69217257-chr4:69223391..69225244,2	MCF-7	breast:
4	chr4:69212213..69214534-chr4:69225131..69226946,2	MCF-7	breast:
5	chr4:69218330..69220312-chr4:69233366..69236029,2	MCF-7	breast:
6	chr4:69215315..69216150-chr4:69241399..69242116,2	MCF-7	breast:
7	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
8	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
9	chr4:69143211..69145096-chr4:69239415..69241951,2	K562	blood:
10	chr4:69218178..69222853-chr4:69225128..69229971,4	MCF-7	breast:
11	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
12	chr4:69227116..69229844-chr4:69232808..69235424,3	MCF-7	breast:
13	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
14	chr4:69211727..69213859-chr4:69233011..69234860,2	MCF-7	breast:
15	chr4:69214098..69215634-chr4:69235366..69237032,2	MCF-7	breast:
16	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
17	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
18	chr4:69218952..69221343-chr4:69221565..69223660,2	K562	blood:
19	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
20	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
21	chr4:69236161..69238300-chr4:69240878..69243749,2	MCF-7	breast:
22	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
23	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
24	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
25	chr4:69218330..69220312-chr4:69233366..69236029,2	MCF-7	breast:
26	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
27	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
28	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
29	chr4:69212970..69215845-chr4:69239349..69242311,2	MCF-7	breast:
30	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
31	chr4:69193668..69196027-chr4:69216381..69218945,2	K562	blood:
32	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
33	chr4:69225743..69228378-chr4:69231035..69233208,2	K562	blood:
34	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
35	chr19:34663114..34663782-chr4:69227413..69228097,2	HCT-116	colon:
36	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
37	chr4:69218178..69222853-chr4:69225128..69229971,4	MCF-7	breast:
38	chr4:69225977..69228923-chr4:69232908..69234757,2	MCF-7	breast:
39	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
40	chr4:69210254..69212514-chr4:69233666..69236534,2	MCF-7	breast:
41	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
42	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
43	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
44	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
45	chr4:69225743..69228378-chr4:69231035..69233208,2	K562	blood:
46	chr4:69227116..69229844-chr4:69232808..69235424,3	MCF-7	breast:
47	chr4:69213603..69215709-chr4:69245624..69247287,2	K562	blood:
48	chr4:69214168..69215842-chr4:69249504..69252039,2	MCF-7	breast:
49	chr4:69225977..69228923-chr4:69232908..69234757,2	MCF-7	breast:
50	chr4:69218952..69221343-chr4:69221565..69223660,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
2	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
5	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
6	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733

No data

Variant related genes	Relation type
TMPRSS11E	TF binding region
MT2P1	TF binding region
YTHDC1	TF binding region
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
TMPRSS11E	CpG island
MT2P1	CpG island
YTHDC1	CpG island
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000257103	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000162840	chromatin interactions
ENSG00000087128	chromatin interactions

Extended variants
information (count: 10463 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:10463 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551207394	chr4:69217774-69217775	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs4860292	chr4:69217820-69217821	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs184837347	chr4:69217983-69217984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575059359	chr4:69217985-69217986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116424604	chr4:69218100-69218101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189979818	chr4:69218148-69218149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555996558	chr4:69218217-69218218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575748435	chr4:69218222-69218223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538054087	chr4:69218241-69218242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558431162	chr4:69218260-69218261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191996627	chr4:69218281-69218282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540412878	chr4:69218327-69218328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540957078	chr4:69218348-69218349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560481704	chr4:69218380-69218381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535878165	chr4:69218437-69218438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374437219	chr4:69218452-69218453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146982277	chr4:69218453-69218454	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532571074	chr4:69218457-69218458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562836998	chr4:69218486-69218487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531871622	chr4:69218487-69218488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551020731	chr4:69218505-69218506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564843959	chr4:69218571-69218572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150971158	chr4:69218587-69218588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs140836104	chr4:69218605-69218606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548208522	chr4:69218654-69218655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs115847717	chr4:69218662-69218663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550332488	chr4:69218689-69218690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535874622	chr4:69218696-69218697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549797484	chr4:69218699-69218700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569642305	chr4:69218719-69218720	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376132970	chr4:69218737-69218738	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs538773930	chr4:69218758-69218759	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184496289	chr4:69218760-69218761	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs34553305	chr4:69218849-69218850	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189279254	chr4:69218865-69218866	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116228728	chr4:69218869-69218870	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs115290845	chr4:69218884-69218885	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150210785	chr4:69218938-69218939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566439883	chr4:69218940-69218941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562934270	chr4:69218945-69218946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576435334	chr4:69218995-69218996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545117842	chr4:69218997-69218998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4860928	chr4:69219049-69219050	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs374212824	chr4:69219068-69219069	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs547244965	chr4:69219091-69219092	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561025126	chr4:69219130-69219131	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs367772976	chr4:69219131-69219132	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs536587898	chr4:69219179-69219180	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530045102	chr4:69219182-69219183	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs549497998	chr4:69219200-69219201	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:1472 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69216000-69219400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:69216400-69224400	Weak transcription	HepG2	liver
3	chr4:69216600-69218200	Weak transcription	Fetal Intestine Large	intestine
4	chr4:69216600-69218200	Weak transcription	Fetal Intestine Small	intestine
5	chr4:69216800-69221800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:69218200-69219200	Enhancers	Fetal Intestine Large	intestine
7	chr4:69218200-69219200	Enhancers	Fetal Intestine Small	intestine
8	chr4:69218400-69218600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:69219200-69224800	Weak transcription	Fetal Intestine Small	intestine
10	chr4:69219200-69225000	Weak transcription	Fetal Intestine Large	intestine
11	chr4:69219400-69219600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:69219600-69227400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:69221800-69222200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:69223400-69223600	Enhancers	Fetal Kidney	kidney
15	chr4:69223600-69228200	Weak transcription	Fetal Kidney	kidney
16	chr4:69224400-69225000	Enhancers	HepG2	liver
17	chr4:69224800-69225200	Enhancers	Fetal Intestine Small	intestine
18	chr4:69224800-69225600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr4:69224800-69225600	Enhancers	GM12878-XiMat	blood
20	chr4:69224800-69227600	Enhancers	Placenta	Placenta
21	chr4:69224800-69228000	Enhancers	NHEK	skin
22	chr4:69225000-69225200	Flanking Active TSS	HepG2	liver
23	chr4:69225000-69225600	Enhancers	Fetal Intestine Large	intestine
24	chr4:69225200-69225400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:69225200-69225400	Active TSS	HepG2	liver
26	chr4:69225200-69225600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr4:69225200-69225600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr4:69225200-69225600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr4:69225200-69225600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr4:69225200-69226600	Weak transcription	Fetal Intestine Small	intestine
31	chr4:69225400-69225600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:69225400-69225800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:69225400-69226600	Weak transcription	HepG2	liver
34	chr4:69225400-69226800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:69225400-69227600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:69225600-69226600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:69225600-69226600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:69225600-69226800	Weak transcription	Fetal Intestine Large	intestine
39	chr4:69225600-69227800	Enhancers	HMEC	breast
40	chr4:69225800-69226800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:69226200-69227800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:69226400-69227400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:69226400-69227600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:69226400-69227800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:69226400-69227800	Enhancers	Hela-S3	cervix
46	chr4:69226600-69227200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:69226600-69227400	Enhancers	Fetal Intestine Small	intestine
48	chr4:69226600-69227400	Enhancers	K562	blood
49	chr4:69226600-69227600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:69226600-69227600	Enhancers	Muscle Satellite Cultured Cells	--

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