Variant report

Variant	rs57490980
Chromosome Location	chr17:18160753-18160754
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:18160689-18160895	GM12878	blood:	n/a	n/a
2	CTCF	chr17:18160660-18160810	SAEC	small airway:	n/a	n/a
3	MXI1	chr17:18160397-18162423	HepG2	liver:	n/a	n/a
4	SMC3	chr17:18160536-18160786	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr17:18160581-18162629	Hela-S3	cervix:	n/a	n/a
6	MYC	chr17:18160728-18160909	MCF-7	breast:	n/a	n/a
7	CTCF	chr17:18160620-18160770	HRPEpiC	eye:	n/a	n/a
8	JUND	chr17:18160549-18162498	H1-hESC	embryonic stem cell:	n/a	n/a
9	NR2F2	chr17:18160434-18162450	MCF-7	breast:	n/a	n/a
10	CTCF	chr17:18160680-18160830	SAEC	small airway:	n/a	n/a
11	ZNF143	chr17:18160536-18160941	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr17:18160620-18160770	HMEC	breast:	n/a	n/a
13	POLR2A	chr17:18160601-18161010	H1-hESC	embryonic stem cell:	n/a	n/a
14	MXI1	chr17:18160692-18162606	IMR90	lung:	n/a	n/a
15	SIN3AK20	chr17:18160340-18162304	MCF-7	breast:	n/a	n/a
16	CTCF	chr17:18160673-18160845	MCF-7	breast:	n/a	n/a
17	FOXA1	chr17:18160454-18160881	T-47D	breast:	n/a	n/a
18	CTCF	chr17:18160640-18160790	AG04449	skin:	n/a	n/a
19	MXI1	chr17:18160652-18162596	SK-N-SH	brain:	n/a	n/a
20	CTCF	chr17:18160676-18160824	H1-hESC	embryonic stem cell:	n/a	n/a
21	HCFC1	chr17:18160707-18162492	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr17:18160645-18162369	MCF-7	breast:	n/a	n/a
23	POLR2A	chr17:18160697-18162602	HepG2	liver:	n/a	n/a
24	CTCF	chr17:18160660-18160810	Hela-S3	cervix:	n/a	n/a
25	RCOR1	chr17:18160693-18160951	HepG2	liver:	n/a	n/a
26	SP1	chr17:18160431-18160896	H1-hESC	embryonic stem cell:	n/a	chr17:18160681-18160692
27	POLR2A	chr17:18160625-18160955	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr17:18160684-18160787	GM12892	blood:	n/a	n/a
29	MAX	chr17:18160473-18162523	MCF-7	breast:	n/a	n/a
30	TEAD4	chr17:18160389-18160900	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr17:18160399-18162709	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr17:18160333-18162468	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr17:18160687-18160771	GM19238	blood:	n/a	n/a
34	CTCF	chr17:18160620-18160770	GM06990	blood:	n/a	n/a
35	CTCF	chr17:18160690-18160804	MCF-7	breast:	n/a	n/a
36	POLR2A	chr17:18160623-18160862	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:18160664-18160856	NHEK	skin:	n/a	n/a
38	SIN3A	chr17:18160457-18162506	H1-hESC	embryonic stem cell:	n/a	chr17:18161345-18161354
39	POLR2A	chr17:18160632-18160983	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr17:18160689-18160879	GM12878	blood:	n/a	n/a
41	POLR2A	chr17:18160335-18162502	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAFK	chr17:18160725-18161051	HepG2	liver:	n/a	n/a
43	SMARCB1	chr17:18160684-18162484	Hela-S3	cervix:	n/a	n/a
44	GTF2F1	chr17:18160440-18160845	H1-hESC	embryonic stem cell:	n/a	n/a
45	WRNIP1	chr17:18160700-18160785	GM12878	blood:	n/a	n/a
46	POLR2A	chr17:18160615-18160784	GM12878	blood:	n/a	n/a
47	TEAD4	chr17:18160464-18161118	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr17:18160699-18160798	GM12891	blood:	n/a	n/a
49	RCOR1	chr17:18160570-18160894	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr17:18160681-18160821	MCF-7	breast:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18085197..18089449-chr17:18160313..18164902,6	K562	blood:
2	chr17:18149206..18150883-chr17:18160011..18162354,3	K562	blood:
3	chr17:18127100..18135567-chr17:18158023..18168767,25	MCF-7	breast:
4	chr17:18156705..18166530-chr17:18215131..18220177,19	MCF-7	breast:
5	chr17:18086032..18088176-chr17:18160313..18162937,3	K562	blood:
6	chr17:18160519..18163064-chr17:57184178..57185847,2	MCF-7	breast:
7	chr17:18126073..18132705-chr17:18158327..18165323,14	MCF-7	breast:
8	chr17:18158849..18161472-chr17:18226331..18228845,2	MCF-7	breast:
9	chr17:18085788..18088045-chr17:18160400..18163100,2	MCF-7	breast:
10	chr17:18160366..18162830-chr17:18217207..18220188,2	K562	blood:
11	chr17:18158589..18161919-chr17:18164225..18167330,4	K562	blood:
12	chr17:18159414..18161817-chr17:18169101..18171467,2	K562	blood:
13	chr17:18135795..18137603-chr17:18160135..18163013,2	MCF-7	breast:
14	chr17:18159194..18166260-chr17:18215929..18222740,16	MCF-7	breast:

No data

Variant related genes	Relation type
FLII	TF binding region
MIEF2	TF binding region
ENSG00000228000	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000131899	Chromatin interaction
ENSG00000177427	Chromatin interaction
ENSG00000237382	Chromatin interaction
ENSG00000177302	Chromatin interaction
ENSG00000267350	Chromatin interaction
ENSG00000177731	Chromatin interaction
ENSG00000260647	Chromatin interaction
ENSG00000266677	Chromatin interaction
ENSG00000091542	Chromatin interaction
ENSG00000176994	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs11078415	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11867855	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11867895	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11868708	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11869515	0.82[EUR][1000 genomes]
rs11869582	0.81[EUR][1000 genomes]
rs11869952	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11871761	0.85[EUR][1000 genomes]
rs11872031	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12449313	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12450760	0.82[EUR][1000 genomes]
rs12451555	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12451698	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12451807	0.81[EUR][1000 genomes]
rs12939851	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16961114	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16961133	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16961153	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1925	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1962949	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1962950	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2071242	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2273029	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2290502	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2290503	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2290504	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2290505	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2294913	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28364628	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35738574	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3817992	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3829956	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3862147	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3889544	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4386179	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4450455	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4500798	0.82[EUR][1000 genomes]
rs4556848	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4925151	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4925177	0.82[EUR][1000 genomes]
rs4925178	0.82[EUR][1000 genomes]
rs57697650	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59366579	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62072507	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62072509	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62072511	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62072515	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62072537	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62072540	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62072541	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62072544	0.82[EUR][1000 genomes]
rs62072545	0.82[EUR][1000 genomes]
rs6502641	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7211573	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7215678	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7405677	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7498	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8081042	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8081155	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8081343	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9901707	0.82[EUR][1000 genomes]
rs9909104	0.82[EUR][1000 genomes]
rs9910090	0.82[EUR][1000 genomes]
rs9913139	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
6	nsv907773	chr17:18099962-18206234	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv907774	chr17:18103907-18206234	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv907775	chr17:18108496-18206234	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv543246	chr17:18121007-18165604	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
10	nsv9503	chr17:18121474-18169166	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
11	nsv907776	chr17:18122485-18170948	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
12	nsv1066718	chr17:18125122-18180807	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv907777	chr17:18131087-18163262	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18159000-18162400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr17:18159200-18160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr17:18159200-18160800	Weak transcription	Fetal Kidney	kidney
4	chr17:18159200-18161000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
5	chr17:18159200-18162000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr17:18159800-18160800	Enhancers	Fetal Heart	heart
7	chr17:18159800-18161000	Enhancers	Small Intestine	intestine
8	chr17:18160000-18160800	Enhancers	Primary B cells from peripheral blood	blood
9	chr17:18160000-18160800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr17:18160000-18160800	Enhancers	Left Ventricle	heart
11	chr17:18160000-18160800	Genic enhancers	Sigmoid Colon	Sigmoid Colon
12	chr17:18160000-18161200	Enhancers	Fetal Brain Male	brain
13	chr17:18160000-18161200	Flanking Active TSS	HMEC	breast
14	chr17:18160000-18161400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr17:18160200-18160800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr17:18160200-18160800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr17:18160200-18160800	Weak transcription	Aorta	Aorta
18	chr17:18160200-18160800	Enhancers	Ovary	ovary
19	chr17:18160200-18160800	Flanking Active TSS	HepG2	liver
20	chr17:18160200-18161000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr17:18160200-18161000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr17:18160200-18161000	Flanking Active TSS	Pancreas	Pancrea
23	chr17:18160200-18161000	Flanking Active TSS	Hela-S3	cervix
24	chr17:18160200-18161000	Flanking Active TSS	HSMM	muscle
25	chr17:18160200-18161200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr17:18160200-18161200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr17:18160200-18161200	Flanking Active TSS	Esophagus	oesophagus
28	chr17:18160200-18161400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr17:18160200-18161400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr17:18160200-18161400	Flanking Active TSS	Colonic Mucosa	Colon
31	chr17:18160200-18161400	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr17:18160200-18161400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr17:18160200-18161600	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr17:18160200-18162400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr17:18160400-18160800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr17:18160400-18160800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr17:18160400-18160800	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
38	chr17:18160400-18160800	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
39	chr17:18160400-18160800	Flanking Active TSS	NHDF-Ad	bronchial
40	chr17:18160400-18161000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr17:18160400-18161000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr17:18160400-18161000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr17:18160400-18161000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr17:18160400-18161000	Flanking Active TSS	Gastric	stomach
45	chr17:18160400-18161000	Flanking Active TSS	Rectal Smooth Muscle	rectum
46	chr17:18160400-18161000	Flanking Active TSS	NHLF	lung
47	chr17:18160400-18161200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
48	chr17:18160400-18161200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr17:18160400-18161200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr17:18160400-18161200	Flanking Active TSS	Colon Smooth Muscle	Colon

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