Variant report

Variant	rs11976063
Chromosome Location	chr7:4831969-4831970
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:4831694-4831997	K562	blood:	n/a	n/a
2	USF2	chr7:4831789-4832032	H1-hESC	embryonic stem cell:	n/a	n/a
3	RAD21	chr7:4831599-4832081	H1-hESC	embryonic stem cell:	n/a	n/a
4	MAX	chr7:4831652-4831985	K562	blood:	n/a	n/a
5	CTCF	chr7:4831820-4831970	GM12864	blood:	n/a	n/a
6	POLR2A	chr7:4831651-4832466	PFSK-1	brain:	n/a	n/a
7	POLR2A	chr7:4831012-4832238	K562	blood:	n/a	n/a
8	CTCF	chr7:4831656-4832057	H1-hESC	embryonic stem cell:	n/a	n/a
9	ZNF143	chr7:4831711-4832029	GM12878	blood:	n/a	n/a
10	MAZ	chr7:4831726-4832026	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:4831790-4832984	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:4831860-4832010	WI-38	lung:	n/a	n/a
13	RAD21	chr7:4831740-4832095	H1-hESC	embryonic stem cell:	n/a	n/a
14	SMC3	chr7:4831708-4831973	K562	blood:	n/a	n/a
15	CTCF	chr7:4831840-4831990	GM12868	blood:	n/a	n/a
16	POLR2A	chr7:4831694-4832965	A549	lung:	n/a	n/a
17	POLR2A	chr7:4831768-4831991	HCT-116	colon:	n/a	n/a
18	YY1	chr7:4831774-4831994	GM12891	blood:	n/a	n/a
19	ZNF143	chr7:4831738-4831996	K562	blood:	n/a	n/a
20	CBX3	chr7:4831686-4832003	K562	blood:	n/a	n/a
21	POLR2A	chr7:4831843-4832206	K562	blood:	n/a	n/a
22	POLR2A	chr7:4831842-4832047	HUVEC	blood vessel:	n/a	n/a
23	EGR1	chr7:4831731-4832004	K562	blood:	n/a	n/a
24	CTCF	chr7:4831741-4831978	Fibrobl	skin:	n/a	n/a
25	CTCF	chr7:4831820-4831970	HUVEC	blood vessel:	n/a	n/a
26	MAZ	chr7:4831782-4832049	HepG2	liver:	n/a	n/a
27	GTF2F1	chr7:4831828-4832216	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:4831840-4831990	HFF-Myc	foreskin:	n/a	n/a
29	POLR2A	chr7:4831603-4832936	HL-60	blood:	n/a	n/a
30	MYC	chr7:4831768-4832064	H1-hESC	embryonic stem cell:	n/a	n/a
31	BHLHE40	chr7:4831699-4831994	K562	blood:	n/a	n/a
32	SIN3AK20	chr7:4831698-4831970	SK-N-SH	brain:	n/a	n/a
33	CTCF	chr7:4831757-4831975	NHEK	skin:	n/a	n/a
34	CTCFL	chr7:4831763-4831978	K562	blood:	n/a	n/a
35	CTCF	chr7:4831820-4831970	GM06990	blood:	n/a	n/a
36	ZNF143	chr7:4831705-4832523	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:4831820-4831970	GM12869	blood:	n/a	n/a
38	POLR2A	chr7:4829576-4831980	GM12878	blood:	n/a	n/a
39	CTCF	chr7:4831339-4832587	SK-N-SH	brain:	n/a	n/a
40	CREB1	chr7:4831642-4832532	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:4831860-4832010	HCM	heart:	n/a	n/a
42	CTCF	chr7:4831820-4831970	AG04449	skin:	n/a	n/a
43	TEAD4	chr7:4831659-4831977	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr7:4831961-4832870	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr7:4831724-4831974	GM13976	blood:	n/a	n/a
46	CTCF	chr7:4831820-4831970	NHLF	lung:	n/a	n/a
47	CTCF	chr7:4831792-4831981	A549	lung:	n/a	n/a
48	POLR2A	chr7:4831132-4832813	GM18951	blood:	n/a	n/a
49	EGR1	chr7:4831771-4832074	K562	blood:	n/a	n/a
50	CTCF	chr7:4831840-4831990	BE2_C	brain:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4815280..4818251-chr7:4830682..4833750,3	MCF-7	breast:
2	chr7:4823905..4827107-chr7:4829333..4833521,4	MCF-7	breast:
3	chr7:4821235..4827640-chr7:4827846..4833141,11	K562	blood:
4	chr7:4831917..4833699-chr7:4922173..4923727,2	K562	blood:
5	chr7:4830470..4833507-chr7:4836339..4839138,4	K562	blood:

No data

Variant related genes	Relation type
MIR4656	TF binding region
ENSG00000157927	Chromatin interaction
ENSG00000242802	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11976296	1.00[CEU][hapmap]
rs12154545	1.00[EUR][1000 genomes]
rs12154622	1.00[EUR][1000 genomes]
rs12154696	1.00[EUR][1000 genomes]
rs12155405	0.97[EUR][1000 genomes]
rs17135086	1.00[CEU][hapmap]
rs17135109	1.00[CEU][hapmap]
rs17135113	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs35684868	0.84[EUR][1000 genomes]
rs6979798	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs73305396	0.90[AFR][1000 genomes]
rs73305400	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73307305	0.87[EUR][1000 genomes]
rs73671925	0.85[EUR][1000 genomes]
rs749405	1.00[EUR][1000 genomes]
rs7781254	0.87[EUR][1000 genomes]
rs7798106	0.92[EUR][1000 genomes]
rs7802515	1.00[CEU][hapmap]
rs7810433	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs907718	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529538	chr7:4509189-5151503	Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv530968	chr7:4572250-5418004	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1031697	chr7:4677463-5241790	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv538704	chr7:4677463-5241790	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv887377	chr7:4730535-4862259	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv887378	chr7:4730535-4929721	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv887380	chr7:4760124-4929721	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv471293	chr7:4764861-4885221	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv887381	chr7:4769030-4880954	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv823994	chr7:4792385-4928328	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
11	nsv887382	chr7:4792762-4880954	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	nsv8033	chr7:4802287-5086597	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	nsv1022678	chr7:4810626-5113387	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
14	nsv538705	chr7:4810626-5113387	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
15	nsv887383	chr7:4817460-4845701	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
16	esv1846003	chr7:4817952-4845248	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
17	nsv605977	chr7:4820581-4841349	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
18	nsv887384	chr7:4820581-4851897	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
19	nsv887385	chr7:4820581-4860835	Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
20	nsv528748	chr7:4820581-5010993	Enhancers Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
21	nsv1029123	chr7:4821734-4919277	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
22	esv1836977	chr7:4823971-4845701	Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
23	nsv887386	chr7:4823971-4852682	Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
24	nsv887387	chr7:4823971-4860835	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
25	nsv887388	chr7:4823971-4880954	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
26	esv1814177	chr7:4825190-4842927	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
27	nsv605978	chr7:4828077-4854592	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
28	esv3407904	chr7:4831051-4833599	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
29	nsv1021170	chr7:4831361-5058033	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
30	nsv538706	chr7:4831361-5058033	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4816000-4832000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:4816200-4832000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:4816200-4834400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:4816600-4834800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:4816800-4834400	Weak transcription	K562	blood
6	chr7:4816800-4834800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:4817200-4832000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:4819800-4832000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:4820200-4832800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:4820200-4832800	Strong transcription	Dnd41	blood
11	chr7:4820400-4832000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:4820400-4832000	Strong transcription	NHLF	lung
13	chr7:4820400-4832200	Strong transcription	Placenta Amnion	Placenta Amnion
14	chr7:4820400-4832400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:4820400-4834400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:4820600-4832800	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr7:4821400-4834600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr7:4821800-4834200	Weak transcription	HSMM	muscle
19	chr7:4823800-4833000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:4826200-4843400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:4826400-4832000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:4826400-4832000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr7:4826400-4832400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:4826400-4832800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr7:4827200-4832000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr7:4828200-4832000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr7:4828200-4832000	Weak transcription	Small Intestine	intestine
28	chr7:4828600-4832000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:4828600-4832400	Weak transcription	HepG2	liver
30	chr7:4828800-4835800	Weak transcription	Fetal Lung	lung
31	chr7:4829800-4832000	Weak transcription	NH-A	brain
32	chr7:4830200-4832200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:4830400-4832000	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr7:4830400-4832000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:4830400-4832800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:4830600-4832000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr7:4830800-4832000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr7:4830800-4832800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:4830800-4832800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:4831000-4832000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:4831000-4832000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:4831000-4832000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr7:4831000-4832800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:4831000-4832800	Genic enhancers	Placenta	Placenta
45	chr7:4831000-4832800	Strong transcription	A549	lung
46	chr7:4831200-4832000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:4831200-4832000	Weak transcription	Left Ventricle	heart
48	chr7:4831200-4832000	Weak transcription	Ovary	ovary
49	chr7:4831200-4832000	Weak transcription	Rectal Smooth Muscle	rectum
50	chr7:4831400-4832000	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links