Variant report

Variant	esv1844093
Chromosome Location	chr6:57374115-57395170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:185)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57392130-57392164	HepG2	liver:	n/a	n/a
2	ATF1	chr6:57388328-57388901	K562	blood:	n/a	n/a
3	ATF1	chr6:57386257-57386379	K562	blood:	n/a	n/a
4	BACH1	chr6:57388299-57388865	K562	blood:	n/a	n/a
5	BHLHE40	chr6:57375272-57375472	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:57381413-57381830	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr6:57390670-57390900	GM12878	blood:	n/a	n/a
8	BRCA1	chr6:57382748-57382761	HepG2	liver:	n/a	n/a
9	CCNT2	chr6:57376252-57377005	K562	blood:	n/a	n/a
10	CEBPB	chr6:57388107-57388603	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:57388199-57388630	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:57380130-57380666	MCF-7	breast:	n/a	chr6:57380307-57380318
13	CEBPB	chr6:57385025-57385073	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:57380136-57380500	HepG2	liver:	n/a	chr6:57380307-57380318
15	CEBPB	chr6:57380194-57380517	H1-hESC	embryonic stem cell:	n/a	chr6:57380307-57380318
16	CEBPB	chr6:57380150-57380500	Hela-S3	cervix:	n/a	chr6:57380307-57380318
17	CEBPB	chr6:57380149-57380488	K562	blood:	n/a	chr6:57380307-57380318
18	CEBPB	chr6:57388224-57388584	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:57380175-57380499	A549	lung:	n/a	chr6:57380307-57380318
20	CEBPB	chr6:57380198-57380376	HepG2	liver:	n/a	chr6:57380307-57380318
21	CEBPB	chr6:57380157-57380496	IMR90	lung:	n/a	chr6:57380307-57380318
22	CEBPB	chr6:57388182-57388630	MCF-7	breast:	n/a	n/a
23	CEBPB	chr6:57380170-57380548	MCF-7	breast:	n/a	chr6:57380307-57380318
24	CHD2	chr6:57386201-57386211	GM12878	blood:	n/a	n/a
25	CTCF	chr6:57382700-57382850	GM12865	blood:	n/a	n/a
26	CTCF	chr6:57380980-57381130	BE2_C	brain:	n/a	n/a
27	CTCF	chr6:57390560-57390710	GM12865	blood:	n/a	n/a
28	CTCF	chr6:57380780-57380930	BE2_C	brain:	n/a	n/a
29	CTCF	chr6:57382680-57382830	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:57380940-57381090	BJ	skin:	n/a	n/a
31	CTCF	chr6:57386800-57386950	GM12873	blood:	n/a	n/a
32	CTCF	chr6:57380840-57380990	NHLF	lung:	n/a	n/a
33	CTCF	chr6:57380800-57380950	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr6:57386700-57386850	HRE	kidney:	n/a	n/a
35	CTCF	chr6:57380765-57381136	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr6:57386089-57386091	K562	blood:	n/a	n/a
37	CTCF	chr6:57380920-57381070	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr6:57386120-57386270	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:57384980-57385130	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr6:57377260-57377410	GM12868	blood:	n/a	n/a
41	CUX1	chr6:57379883-57380143	GM12878	blood:	n/a	n/a
42	CUX1	chr6:57386096-57386567	GM12878	blood:	n/a	n/a
43	CUX1	chr6:57376799-57377094	GM12878	blood:	n/a	n/a
44	CUX1	chr6:57392551-57392552	GM12878	blood:	n/a	n/a
45	CUX1	chr6:57374920-57375483	GM12878	blood:	n/a	n/a
46	CUX1	chr6:57385965-57386150	K562	blood:	n/a	n/a
47	E2F4	chr6:57375255-57375482	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr6:57392605-57392997	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr6:57380317-57380746	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr6:57390828-57391397	MCF10A-Er-Src	breast:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57391815-57391865	AG04449	skin:	fetal
2	chr6:57391815-57391865	HRPEpiC	eye:	n/a
3	chr6:57391815-57391865	AG04449	skin:	fetal
4	chr6:57391815-57391865	HRPEpiC	eye:	n/a
5	chr6:57391815-57391865	SK-N-SH	brain:	n/a
6	chr6:57384347-57384397	U87	brain:	n/a
7	chr6:57384347-57384397	GM19239	blood:	n/a
8	chr6:57384347-57384397	HUVEC	blood vessel:	n/a
9	chr6:57391815-57391865	SKMC	muscle:	n/a
10	chr6:57391815-57391865	ECC-1	luminal epithelium:	n/a
11	chr6:57391815-57391865	Hepatocyte	liver:	n/a
12	chr6:57391815-57391865	HepG2	liver:	n/a
13	chr6:57384347-57384397	AG04450	lung:	fetal
14	chr6:57385844-57385894	NB4	blood:	n/a
15	chr6:57384347-57384397	HRPEpiC	eye:	n/a
16	chr6:57384347-57384397	IMR90	lung:	fetal
17	chr6:57385844-57385894	T-47D	breast:	n/a
18	chr6:57391815-57391865	SAEC	small airway:	n/a
19	chr6:57384347-57384397	PFSK-1	brain:	n/a
20	chr6:57384347-57384397	T-47D	breast:	n/a
21	chr6:57391815-57391865	NT2-D1	testis:	n/a
22	chr6:57385844-57385894	GM12891	blood:	n/a
23	chr6:57391815-57391865	PFSK-1	brain:	n/a
24	chr6:57391815-57391865	RPTEC	kidney:	n/a
25	chr6:57385844-57385894	HIPEpiC	eye:	n/a
26	chr6:57391815-57391865	SK-N-MC	brain:	n/a
27	chr6:57391815-57391865	AG10803	skin:	n/a
28	chr6:57384347-57384397	AG04449	skin:	fetal
29	chr6:57385844-57385894	AoSMC	blood vessel:	n/a
30	chr6:57384347-57384397	HRCEpiC	kidney:	n/a
31	chr6:57391815-57391865	PrEC	prostate:	n/a
32	chr6:57391815-57391865	HCT-116	colon:	n/a
33	chr6:57384347-57384397	NT2-D1	testis:	n/a
34	chr6:57385844-57385894	HCPEpiC	choroid plexus:	n/a
35	chr6:57384347-57384397	HCPEpiC	choroid plexus:	n/a
36	chr6:57391815-57391865	GM12878	blood:	n/a
37	chr6:57385844-57385894	ECC-1	luminal epithelium:	n/a
38	chr6:57384347-57384397	AG09309	skin:	n/a
39	chr6:57391815-57391865	CMK	blood:	n/a
40	chr6:57384347-57384397	SKMC	muscle:	n/a
41	chr6:57391815-57391865	HEK293	kidney:	embryo
42	chr6:57385844-57385894	AG04449	skin:	fetal
43	chr6:57385844-57385894	BJ	skin:	n/a
44	chr6:57391815-57391865	GM19239	blood:	n/a
45	chr6:57384347-57384397	NHDF-neo	bronchial:	n/a
46	chr6:57385844-57385894	HAEpiC	amniotic membrane:	n/a
47	chr6:57385844-57385894	NH-A	brain:	n/a
48	chr6:57391815-57391865	AG04450	lung:	fetal
49	chr6:57384347-57384397	MCF10A-Er-Src	breast:	n/a
50	chr6:57385844-57385894	SKMC	muscle:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:57394320..57396660-chr6:58286293..58287831,2	MCF-7	breast:
2	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
3	chr6:57368098..57370585-chr6:57379961..57384432,3	K562	blood:
4	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
5	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
6	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
7	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
8	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
9	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
10	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:

No data

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

Extended variants
information (count: 1276 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2397476	chr6:57374115-57374116	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199709620	chr6:57374127-57374128	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74998342	chr6:57374140-57374141	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74779909	chr6:57374143-57374144	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541194726	chr6:57374152-57374153	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559568724	chr6:57374154-57374155	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs80251130	chr6:57374172-57374173	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74599805	chr6:57374232-57374233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2397477	chr6:57374242-57374243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2894900	chr6:57374244-57374245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs3805793	chr6:57374252-57374253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs78781001	chr6:57374266-57374267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75998880	chr6:57374289-57374290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78855561	chr6:57374298-57374299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4518499	chr6:57374299-57374300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9464514	chr6:57374330-57374331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75332238	chr6:57374364-57374365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79378061	chr6:57374381-57374382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79214008	chr6:57374394-57374395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs80076643	chr6:57374422-57374423	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs62400920	chr6:57374475-57374476	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs62400921	chr6:57374495-57374496	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs542331674	chr6:57374512-57374513	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs62400922	chr6:57374520-57374521	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs563816124	chr6:57374521-57374522	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs530887060	chr6:57374557-57374558	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs111581946	chr6:57374574-57374575	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs75849188	chr6:57374587-57374588	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs77621742	chr6:57374599-57374600	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs79549793	chr6:57374616-57374617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564765517	chr6:57374620-57374621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72877198	chr6:57374624-57374625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78164739	chr6:57374654-57374655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs33925255	chr6:57374679-57374680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs68070834	chr6:57374680-57374681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566447038	chr6:57374688-57374689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116293302	chr6:57374696-57374697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72877201	chr6:57374704-57374705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528802849	chr6:57374716-57374717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs74362087	chr6:57374717-57374718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115831928	chr6:57374728-57374729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72877202	chr6:57374729-57374730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546925159	chr6:57374741-57374742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs55878218	chr6:57374749-57374750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs192992062	chr6:57374762-57374763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570789346	chr6:57374776-57374777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57956455	chr6:57374778-57374779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34543926	chr6:57374804-57374805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77059671	chr6:57374807-57374808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs60311101	chr6:57374810-57374811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	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
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57370400-57374200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:57370400-57380200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:57371600-57375400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:57372400-57374400	Weak transcription	Left Ventricle	heart
5	chr6:57372600-57379600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:57373600-57374200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr6:57373600-57374200	ZNF genes & repeats	NHDF-Ad	bronchial
8	chr6:57373800-57377200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr6:57374200-57374600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:57374400-57374600	ZNF genes & repeats	Left Ventricle	heart
11	chr6:57374400-57376600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:57374600-57375400	Weak transcription	Left Ventricle	heart
13	chr6:57374600-57376400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:57375000-57375600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:57375200-57375600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:57375200-57375800	Enhancers	Brain Germinal Matrix	brain
17	chr6:57375400-57375600	Enhancers	Left Ventricle	heart
18	chr6:57375600-57380600	Weak transcription	Left Ventricle	heart
19	chr6:57375800-57376000	Enhancers	Fetal Brain Male	brain
20	chr6:57376400-57376600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:57376600-57380800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:57379200-57379400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr6:57379200-57381400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr6:57379400-57380800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr6:57379600-57383400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:57379800-57380800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:57380200-57381400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr6:57380200-57381600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:57380200-57383600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:57380200-57383800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr6:57380400-57381800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr6:57380400-57383800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:57380800-57381200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:57380800-57381200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:57380800-57381200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:57380800-57381200	ZNF genes & repeats	Left Ventricle	heart
37	chr6:57380800-57381400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:57380800-57381400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr6:57380800-57381400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:57381000-57381200	Bivalent Enhancer	Aorta	Aorta
41	chr6:57381200-57382600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:57381200-57382600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr6:57381200-57382600	Weak transcription	Left Ventricle	heart
44	chr6:57381200-57384800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr6:57381400-57382600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr6:57381400-57382600	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr6:57381400-57382600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:57381400-57382800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr6:57381400-57383200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr6:57381600-57382000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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