Variant report

Variant	rs267600961
Chromosome Location	chr6:31743984-31743985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr6:31743526-31746220	K562	blood:	n/a	chr6:31745138-31745146 chr6:31745650-31745658
2	NR2F2	chr6:31743692-31746295	K562	blood:	n/a	n/a
3	HA-E2F1	chr6:31743607-31744114	MCF-7	breast:	n/a	n/a
4	POLR2A	chr6:31743893-31745896	K562	blood:	n/a	n/a
5	POLR2A	chr6:31743241-31751112	K562	blood:	n/a	n/a
6	POLR2A	chr6:31742851-31744026	MCF-7	breast:	n/a	n/a
7	BHLHE40	chr6:31743765-31744030	HepG2	liver:	n/a	n/a
8	TCF7L2	chr6:31743727-31744036	MCF-7	breast:	n/a	chr6:31743862-31743876
9	CHD2	chr6:31743828-31746134	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31743952-31744002	HRE	kidney:	n/a
2	chr6:31743952-31744002	NH-A	brain:	n/a
3	chr6:31743961-31744011	HepG2	liver:	n/a
4	chr6:31743952-31744002	GM12892	blood:	n/a
5	chr6:31743952-31744002	LNCaP	prostate:	n/a
6	chr6:31743961-31744011	A549	lung:	n/a
7	chr6:31743961-31744011	HCF	heart:	n/a
8	chr6:31743952-31744002	HRCEpiC	kidney:	n/a
9	chr6:31743961-31744011	PFSK-1	brain:	n/a
10	chr6:31743952-31744002	PANC-1	pancreas:	n/a
11	chr6:31743952-31744002	HepG2	liver:	n/a
12	chr6:31743952-31744002	RPTEC	kidney:	n/a
13	chr6:31743961-31744011	SKMC	muscle:	n/a
14	chr6:31743961-31744011	HUVEC	blood vessel:	n/a
15	chr6:31743952-31744002	ovcar-3	ovarian:	n/a
16	chr6:31743952-31744002	NB4	blood:	n/a
17	chr6:31743952-31744002	AG10803	skin:	n/a
18	chr6:31743961-31744011	H1-hESC	embryonic stem cell:	embryo
19	chr6:31743961-31744011	HEEpiC	esophagus:	n/a
20	chr6:31743961-31744011	GM19239	blood:	n/a
21	chr6:31743961-31744011	HIPEpiC	eye:	n/a
22	chr6:31743952-31744002	AoSMC	blood vessel:	n/a
23	chr6:31743961-31744011	ovcar-3	ovarian:	n/a
24	chr6:31743952-31744002	HEK293	kidney:	embryo
25	chr6:31743961-31744011	PrEC	prostate:	n/a
26	chr6:31743952-31744002	IMR90	lung:	fetal
27	chr6:31743952-31744002	SK-N-SH	brain:	n/a
28	chr6:31743961-31744011	K562	blood:	n/a
29	chr6:31743961-31744011	HL-60	blood:	n/a
30	chr6:31743961-31744011	NB4	blood:	n/a
31	chr6:31743952-31744002	NHBE	bronchial:	n/a
32	chr6:31743961-31744011	AG04449	skin:	fetal
33	chr6:31743961-31744011	Jurkat	blood:	n/a
34	chr6:31743961-31744011	GM06990	blood:	n/a
35	chr6:31743961-31744011	IMR90	lung:	fetal
36	chr6:31743961-31744011	NHDF-neo	bronchial:	n/a
37	chr6:31743952-31744002	BJ	skin:	n/a
38	chr6:31743952-31744002	PFSK-1	brain:	n/a
39	chr6:31743952-31744002	HCPEpiC	choroid plexus:	n/a
40	chr6:31743952-31744002	SAEC	small airway:	n/a
41	chr6:31743952-31744002	HCM	heart:	n/a
42	chr6:31743961-31744011	RPTEC	kidney:	n/a
43	chr6:31743952-31744002	GM12878	blood:	n/a
44	chr6:31743961-31744011	LNCaP	prostate:	n/a
45	chr6:31743961-31744011	ECC-1	luminal epithelium:	n/a
46	chr6:31743961-31744011	CMK	blood:	n/a
47	chr6:31743952-31744002	ProgFib	skin:	n/a
48	chr6:31743961-31744011	HAEpiC	amniotic membrane:	n/a
49	chr6:31743952-31744002	U87	brain:	n/a
50	chr6:31743952-31744002	A549	lung:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31508578..31511041-chr6:31743489..31745514,2	K562	blood:
2	chr6:31710678..31714958-chr6:31739473..31744061,4	MCF-7	breast:
3	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
4	chr6:31697592..31699245-chr6:31742808..31745377,2	MCF-7	breast:
5	chr6:31742931..31744824-chr6:31926408..31928564,2	K562	blood:
6	chr6:31632664..31635327-chr6:31741807..31745187,4	MCF-7	breast:
7	chr6:31743287..31747076-chr6:31793437..31796925,5	MCF-7	breast:
8	chr6:31701475..31705916-chr6:31741171..31744372,4	MCF-7	breast:
9	chr6:31742555..31745004-chr6:31773789..31777145,5	MCF-7	breast:
10	chr6:31642643..31644341-chr6:31742570..31744549,2	MCF-7	breast:
11	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
12	chr6:31696116..31699055-chr6:31743914..31747307,3	MCF-7	breast:
13	chr6:31743107..31747994-chr6:31781956..31785553,7	MCF-7	breast:
14	chr11:64545106..64547042-chr6:31742109..31744042,2	MCF-7	breast:
15	chr6:31668602..31672513-chr6:31741310..31744822,4	MCF-7	breast:
16	chr6:31508667..31511581-chr6:31742885..31745171,3	MCF-7	breast:
17	chr6:31507944..31511146-chr6:31743964..31746169,3	K562	blood:
18	chr6:31502088..31504001-chr6:31743213..31745224,2	MCF-7	breast:
19	chr6:31739355..31742514-chr6:31742775..31744985,3	MCF-7	breast:
20	chr6:31741149..31744902-chr6:31760858..31763694,5	MCF-7	breast:
21	chr6:31737503..31739335-chr6:31742183..31744187,2	MCF-7	breast:
22	chr6:31742944..31744994-chr6:31869511..31871431,2	K562	blood:
23	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
24	chr6:31743176..31746587-chr6:31939802..31942689,4	K562	blood:
25	chr6:31742934..31744615-chr6:31773250..31774889,2	MCF-7	breast:

No data

Variant related genes	Relation type
VWA7	TF binding region
VWA7	CpG island
ENSG00000204387	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000168066	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204410	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
10	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
11	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
12	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
13	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
15	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS 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 lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
16	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
17	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
18	nsv884431	chr6:31732679-31761386	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
19	nsv601943	chr6:31733544-31763862	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	55 gene(s)	inside rSNPs	diseases
20	nsv884432	chr6:31734117-31777687	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
21	nsv884433	chr6:31737701-31777687	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
22	nsv884434	chr6:31739881-31748110	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	33 gene(s)	inside rSNPs	diseases
23	nsv884435	chr6:31739881-31750919	Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	34 gene(s)	inside rSNPs	diseases
24	nsv884436	chr6:31739881-31754096	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	35 gene(s)	inside rSNPs	diseases
25	nsv884437	chr6:31739881-31777687	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
26	nsv884438	chr6:31742590-31751832	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	32 gene(s)	inside rSNPs	diseases
27	nsv884439	chr6:31742590-31754096	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	33 gene(s)	inside rSNPs	diseases
28	nsv884440	chr6:31743882-31775984	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
29	esv3370799	chr6:31743973-31748071	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31716600-31744000	Weak transcription	GM12878-XiMat	blood
2	chr6:31731400-31744400	Weak transcription	Left Ventricle	heart
3	chr6:31731800-31749600	Weak transcription	HUVEC	blood vessel
4	chr6:31732600-31745000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:31732800-31744400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:31734600-31744200	Weak transcription	Brain Anterior Caudate	brain
7	chr6:31734600-31744200	Weak transcription	NH-A	brain
8	chr6:31734600-31744600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr6:31734600-31744600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:31734600-31745200	Weak transcription	Brain Germinal Matrix	brain
11	chr6:31734600-31745400	Weak transcription	Fetal Brain Female	brain
12	chr6:31734600-31746600	Weak transcription	Brain Angular Gyrus	brain
13	chr6:31734800-31745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:31737200-31744200	Weak transcription	Fetal Stomach	stomach
15	chr6:31737400-31744400	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:31737400-31744600	Enhancers	Primary T cells fromperipheralblood	blood
17	chr6:31738000-31744200	Weak transcription	Primary B cells from cord blood	blood
18	chr6:31738800-31745800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr6:31739800-31746000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr6:31740200-31744800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:31740400-31744200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr6:31740400-31744600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:31741000-31744400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:31741000-31744400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr6:31741000-31744400	Weak transcription	Brain Hippocampus Middle	brain
26	chr6:31741000-31744800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:31741000-31745600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr6:31741200-31744000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:31741200-31744200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr6:31741200-31744400	Weak transcription	Fetal Thymus	thymus
31	chr6:31741200-31744800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:31741200-31744800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr6:31741200-31745800	Weak transcription	Brain Substantia Nigra	brain
34	chr6:31741400-31744400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:31741400-31744400	Weak transcription	Primary T cells from cord blood	blood
36	chr6:31741400-31745600	Weak transcription	Dnd41	blood
37	chr6:31741800-31744400	Enhancers	K562	blood
38	chr6:31741800-31745400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:31741800-31745600	Enhancers	Placenta	Placenta
40	chr6:31742200-31744200	Enhancers	Hela-S3	cervix
41	chr6:31742400-31744000	Weak transcription	Thymus	Thymus
42	chr6:31742400-31744600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:31742600-31746000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr6:31742800-31744200	Enhancers	Duodenum Mucosa	Duodenum
45	chr6:31742800-31744400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:31742800-31744400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:31742800-31744400	Enhancers	Colonic Mucosa	Colon
48	chr6:31742800-31744400	Enhancers	Fetal Intestine Large	intestine
49	chr6:31742800-31744400	Enhancers	A549	lung
50	chr6:31742800-31744800	Enhancers	Placenta Amnion	Placenta Amnion

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