Variant report

Variant	nsv885915
Chromosome Location	chr6:57249977-57422878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1857)
CpG islands
(count:734)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57364923-57365929	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:57392130-57392164	HepG2	liver:	n/a	n/a
3	ATF1	chr6:57386257-57386379	K562	blood:	n/a	n/a
4	ATF1	chr6:57296724-57296768	K562	blood:	n/a	n/a
5	ATF1	chr6:57422764-57422956	K562	blood:	n/a	n/a
6	ATF1	chr6:57414346-57414465	K562	blood:	n/a	n/a
7	ATF1	chr6:57329848-57330048	K562	blood:	n/a	n/a
8	ATF1	chr6:57388328-57388901	K562	blood:	n/a	n/a
9	ATF2	chr6:57288167-57288786	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr6:57288321-57288802	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:57337567-57337643	K562	blood:	n/a	n/a
12	BACH1	chr6:57388299-57388865	K562	blood:	n/a	n/a
13	BACH1	chr6:57419536-57419915	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:57334050-57334159	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:57288493-57288790	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:57305657-57305828	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:57365814-57365865	K562	blood:	n/a	n/a
18	BACH1	chr6:57350106-57350125	K562	blood:	n/a	n/a
19	BACH1	chr6:57269047-57269216	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:57363671-57363854	K562	blood:	n/a	n/a
21	BACH1	chr6:57408878-57409078	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:57364094-57364109	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr6:57254076-57254287	GM12878	blood:	n/a	chr6:57254189-57254200
24	BCL11A	chr6:57288294-57288755	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr6:57284786-57285093	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:57284708-57285068	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:57288290-57288688	H1-hESC	embryonic stem cell:	n/a	n/a
28	BHLHE40	chr6:57396741-57396999	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:57284768-57285156	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:57298227-57298377	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:57375272-57375472	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:57268781-57268800	K562	blood:	n/a	n/a
33	BHLHE40	chr6:57395851-57396136	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:57382748-57382761	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:57420502-57420568	GM12878	blood:	n/a	n/a
36	BRCA1	chr6:57420189-57420208	GM12878	blood:	n/a	n/a
37	BRCA1	chr6:57381413-57381830	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr6:57390670-57390900	GM12878	blood:	n/a	n/a
39	BRCA1	chr6:57412393-57412615	GM12878	blood:	n/a	n/a
40	BRCA1	chr6:57398324-57398744	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr6:57370484-57370781	GM12878	blood:	n/a	n/a
42	CBX3	chr6:57253942-57254357	HCT-116	colon:	n/a	n/a
43	CCNT2	chr6:57249858-57249985	K562	blood:	n/a	n/a
44	CCNT2	chr6:57376252-57377005	K562	blood:	n/a	n/a
45	CCNT2	chr6:57337935-57338250	K562	blood:	n/a	n/a
46	CCNT2	chr6:57354598-57355019	K562	blood:	n/a	n/a
47	CEBPB	chr6:57380198-57380376	HepG2	liver:	n/a	chr6:57380307-57380318
48	CEBPB	chr6:57342549-57342911	H1-hESC	embryonic stem cell:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
49	CEBPB	chr6:57380170-57380548	MCF-7	breast:	n/a	chr6:57380307-57380318
50	CEBPB	chr6:57351508-57351781	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57384347-57384397	HEK293	kidney:	embryo
2	chr6:57359134-57359184	GM12891	blood:	n/a
3	chr6:57384347-57384397	HEK293	kidney:	embryo
4	chr6:57359134-57359184	GM12891	blood:	n/a
5	chr6:57350270-57350320	Hepatocyte	liver:	n/a
6	chr6:57339858-57339908	CMK	blood:	n/a
7	chr6:57288411-57288461	AG09309	skin:	n/a
8	chr6:57385844-57385894	HCF	heart:	n/a
9	chr6:57359134-57359184	U87	brain:	n/a
10	chr6:57384347-57384397	SK-N-SH	brain:	n/a
11	chr6:57272398-57272448	Caco-2	colon:	n/a
12	chr6:57391815-57391865	MCF-7	breast:	n/a
13	chr6:57253598-57253648	HAEpiC	amniotic membrane:	n/a
14	chr6:57391815-57391865	HRCEpiC	kidney:	n/a
15	chr6:57385844-57385894	BJ	skin:	n/a
16	chr6:57306409-57306459	GM12891	blood:	n/a
17	chr6:57335405-57335455	BJ	skin:	n/a
18	chr6:57385844-57385894	Hepatocyte	liver:	n/a
19	chr6:57335405-57335455	AG04449	skin:	fetal
20	chr6:57350270-57350320	LNCaP	prostate:	n/a
21	chr6:57339858-57339908	HIPEpiC	eye:	n/a
22	chr6:57391815-57391865	H1-hESC	embryonic stem cell:	embryo
23	chr6:57335405-57335455	HMEC	breast:	n/a
24	chr6:57391815-57391865	BE2_C	brain:	n/a
25	chr6:57391815-57391865	AG10803	skin:	n/a
26	chr6:57305889-57305939	PrEC	prostate:	n/a
27	chr6:57339858-57339908	HRCEpiC	kidney:	n/a
28	chr6:57350270-57350320	HMEC	breast:	n/a
29	chr6:57391815-57391865	PANC-1	pancreas:	n/a
30	chr6:57335405-57335455	ECC-1	luminal epithelium:	n/a
31	chr6:57359134-57359184	BJ	skin:	n/a
32	chr6:57288411-57288461	PANC-1	pancreas:	n/a
33	chr6:57253598-57253648	BJ	skin:	n/a
34	chr6:57339858-57339908	SK-N-MC	brain:	n/a
35	chr6:57305889-57305939	AG10803	skin:	n/a
36	chr6:57339858-57339908	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:57339858-57339908	AG09309	skin:	n/a
38	chr6:57272398-57272448	ECC-1	luminal epithelium:	n/a
39	chr6:57385844-57385894	LNCaP	prostate:	n/a
40	chr6:57305889-57305939	NH-A	brain:	n/a
41	chr6:57272398-57272448	SAEC	small airway:	n/a
42	chr6:57305889-57305939	GM06990	blood:	n/a
43	chr6:57359134-57359184	GM12892	blood:	n/a
44	chr6:57335405-57335455	NT2-D1	testis:	n/a
45	chr6:57385844-57385894	AG09319	gingival:	n/a
46	chr6:57339858-57339908	HRE	kidney:	n/a
47	chr6:57384347-57384397	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:57359134-57359184	PANC-1	pancreas:	n/a
49	chr6:57272398-57272448	AG09319	gingival:	n/a
50	chr6:57359134-57359184	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
2	chr6:57293162..57295571-chr6:57300739..57302981,3	K562	blood:
3	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
4	chr6:57293162..57295571-chr6:57300739..57302981,3	K562	blood:
5	chr6:57396857..57397774-chr9:95368803..95369303,2	MCF-7	breast:
6	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
7	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
8	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
9	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:
10	chr6:57287892..57290689-chr6:57302857..57304913,2	K562	blood:
11	chr6:57394320..57396660-chr6:58286293..58287831,2	MCF-7	breast:
12	chr6:57296504..57298287-chr6:57300033..57301535,2	K562	blood:
13	chr6:57285506..57287843-chr6:57289585..57292088,2	MCF-7	breast:
14	chr6:57368098..57370585-chr6:57379961..57384432,3	K562	blood:
15	chr6:57297598..57300578-chr6:57301764..57305557,4	K562	blood:
16	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
17	chr6:57285506..57287843-chr6:57289585..57292088,2	MCF-7	breast:
18	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
19	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
20	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
21	chr6:57296504..57298287-chr6:57300033..57301535,2	K562	blood:
22	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
23	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
24	chr6:57287892..57290689-chr6:57302857..57304913,2	K562	blood:
25	chr6:57421846..57424167-chr6:57427801..57430462,3	MCF-7	breast:
26	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
27	chr6:57297690..57300107-chr6:57303137..57305465,2	MCF-7	breast:
28	chr6:57297598..57300578-chr6:57301764..57305557,4	K562	blood:
29	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
30	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
31	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
32	chr6:57349293..57351634-chr6:57356907..57359151,3	MCF-7	breast:
33	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
34	chr6:57297690..57300107-chr6:57303137..57305465,2	MCF-7	breast:
35	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
36	chr6:57361390..57363831-chr6:57368584..57370615,2	MCF-7	breast:
37	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:
38	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
39	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
40	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
41	chr6:57244329..57246093-chr6:57248866..57250667,2	K562	blood:
42	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
43	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
44	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-1	chr6:57358736-57358845	ENSG00000266579.1
2	lnc-BAG2-1	chr6:57362331-57362565	ENSG00000266579.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548u	chr6:57254978-57255000	MIMAT0015013

No data

Variant related genes	Relation type
MIR548U	TF binding region
PRIM2	TF binding region
ENSG00000266579	TF binding region
MIR548U	CpG island
PRIM2	CpG island
ENSG00000266579	CpG island
ENSG00000215190	chromatin interactions
ENSG00000146143	chromatin interactions
ENSG00000266579	chromatin interactions

Extended variants
information (count: 10361 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:10361 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4288209	chr6:57249977-57249978	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11962886	chr6:57249995-57249996	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4478411	chr6:57250045-57250046	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
4	rs57977874	chr6:57250054-57250055	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs56133550	chr6:57250056-57250057	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536792819	chr6:57250062-57250063	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs67180682	chr6:57250114-57250115	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558115924	chr6:57250134-57250135	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575762574	chr6:57250155-57250156	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186106363	chr6:57250162-57250163	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534882357	chr6:57250166-57250167	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552999154	chr6:57250237-57250238	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574526314	chr6:57250238-57250239	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs4481432	chr6:57250262-57250263	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7771695	chr6:57250301-57250302	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7771859	chr6:57250318-57250319	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7753846	chr6:57250338-57250339	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557232873	chr6:57250353-57250354	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12201359	chr6:57250357-57250358	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs6916928	chr6:57250388-57250389	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6459210	chr6:57250401-57250402	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6459211	chr6:57250452-57250453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10949038	chr6:57250470-57250471	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546347617	chr6:57250484-57250485	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372139708	chr6:57250543-57250544	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573174142	chr6:57250549-57250550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4526197	chr6:57250593-57250594	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4481433	chr6:57250597-57250598	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs540882161	chr6:57250630-57250631	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12215092	chr6:57250674-57250675	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4342413	chr6:57250696-57250697	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13203462	chr6:57250721-57250722	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4294005	chr6:57250722-57250723	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562247635	chr6:57250736-57250737	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529639228	chr6:57250747-57250748	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78955935	chr6:57250796-57250797	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4593367	chr6:57250823-57250824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375121054	chr6:57250860-57250861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368573080	chr6:57250873-57250874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550755370	chr6:57250914-57250915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4526198	chr6:57250934-57250935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562779450	chr6:57250943-57250944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4295487	chr6:57250949-57250950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191720271	chr6:57250996-57250997	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs530503129	chr6:57251000-57251001	Weak transcription ZNF genes & repeats Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs72871636	chr6:57251012-57251013	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs200925227	chr6:57251025-57251026	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112259196	chr6:57251027-57251028	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200191544	chr6:57251038-57251039	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs149538599	chr6:57251044-57251045	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57199800-57251000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:57236800-57251000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:57238400-57261000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr6:57241200-57254800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:57241200-57262600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:57242800-57259800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:57243000-57250600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr6:57243200-57250400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:57243200-57254200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:57243600-57250600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:57243600-57251400	Weak transcription	Small Intestine	intestine
12	chr6:57243600-57254800	Weak transcription	NH-A	brain
13	chr6:57244400-57259200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:57244800-57252200	Strong transcription	Dnd41	blood
15	chr6:57245200-57251400	Weak transcription	Gastric	stomach
16	chr6:57245200-57257000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:57245400-57250000	Weak transcription	Esophagus	oesophagus
18	chr6:57245400-57250400	Weak transcription	Pancreas	Pancrea
19	chr6:57245400-57250600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:57245400-57251200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:57245400-57253200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:57245400-57253600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:57245400-57254600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr6:57245600-57251000	Weak transcription	Thymus	Thymus
25	chr6:57245600-57253600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:57245600-57254800	Weak transcription	Adipose Nuclei	Adipose
27	chr6:57245600-57256200	Weak transcription	Fetal Intestine Large	intestine
28	chr6:57245600-57261200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:57245800-57253200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:57245800-57254000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr6:57245800-57254800	Weak transcription	Fetal Thymus	thymus
32	chr6:57245800-57256000	Weak transcription	Fetal Brain Male	brain
33	chr6:57246000-57250400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr6:57246000-57251200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:57246000-57251600	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr6:57246000-57252600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr6:57246000-57253600	Weak transcription	GM12878-XiMat	blood
38	chr6:57246000-57254000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:57246000-57255200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr6:57246000-57255400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:57246000-57255400	Weak transcription	Fetal Kidney	kidney
42	chr6:57246200-57250000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:57247000-57254000	Weak transcription	NHLF	lung
44	chr6:57247000-57261200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:57247600-57255200	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr6:57247600-57258000	Weak transcription	Primary B cells from cord blood	blood
47	chr6:57247600-57259800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:57248000-57258200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:57248200-57252000	Weak transcription	Hela-S3	cervix
50	chr6:57248200-57252400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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