Variant report

Variant	rs4871041
Chromosome Location	chr8:121136584-121136585
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:121136567-121136717	GM12892	blood:	n/a	chr8:121136567-121136576
2	CTCF	chr8:121136560-121136710	K562	blood:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
3	CTCF	chr8:121136560-121136710	HCM	heart:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
4	CTCF	chr8:121136560-121136710	HA-sp	spinal cord:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
5	CTCF	chr8:121135475-121137050	A549	lung:	n/a	chr8:121135885-121135903 chr8:121135890-121135898 chr8:121136520-121136528 chr8:121135886-121135902 chr8:121136563-121136576 chr8:121136567-121136576 chr8:121135887-121135908
6	CTCF	chr8:121136540-121136690	GM06990	blood:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
7	CTCF	chr8:121136560-121136710	GM12874	blood:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
8	MAX	chr8:121135781-121136669	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:121136507-121136778	SK-N-SH_RA	brain:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
10	CTCF	chr8:121136560-121136710	AG09319	gingival:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
11	CTCF	chr8:121136560-121136710	NHLF	lung:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
12	CTCF	chr8:121136560-121136710	HRE	kidney:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
13	CTCF	chr8:121136560-121136710	Hela-S3	cervix:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
14	KAP1	chr8:121135761-121136991	U2OS	brain:	n/a	n/a
15	HA-E2F1	chr8:121135682-121137498	MCF-7	breast:	n/a	chr8:121136945-121136960 chr8:121135999-121136006
16	CTCF	chr8:121136580-121136730	GM06990	blood:	n/a	n/a
17	RAD21	chr8:121136317-121137008	MCF-7	breast:	n/a	chr8:121136562-121136575 chr8:121136556-121136570
18	CTCF	chr8:121135611-121136904	HCT-116	colon:	n/a	chr8:121135885-121135903 chr8:121135890-121135898 chr8:121136520-121136528 chr8:121135886-121135902 chr8:121136563-121136576 chr8:121136567-121136576 chr8:121135887-121135908
19	CTCF	chr8:121136554-121136710	K562	blood:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
20	CTCF	chr8:121136421-121136740	T-47D	breast:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
21	CTCF	chr8:121136560-121136710	HCFaa	heart:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
22	ZNF263	chr8:121135781-121137800	HEK293-T-REx	kidney:	n/a	chr8:121137225-121137234
23	E2F6	chr8:121135693-121138879	H1-hESC	embryonic stem cell:	n/a	chr8:121137881-121137893 chr8:121137485-121137500 chr8:121136945-121136960 chr8:121137763-121137771 chr8:121137763-121137771 chr8:121135999-121136006 chr8:121137762-121137772 chr8:121138376-121138385
24	CTCF	chr8:121136532-121136745	SK-N-SH_RA	brain:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
25	CTCF	chr8:121136480-121136630	GM12872	blood:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
26	CTCF	chr8:121136560-121136710	HPF	lung:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
27	CTCF	chr8:121136520-121136670	Hela-S3	cervix:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
28	CTCF	chr8:121135477-121137040	SK-N-SH	brain:	n/a	chr8:121135885-121135903 chr8:121135890-121135898 chr8:121136520-121136528 chr8:121135886-121135902 chr8:121136563-121136576 chr8:121136567-121136576 chr8:121135887-121135908
29	CTCF	chr8:121136580-121136730	HMF	breast:	n/a	n/a
30	CTCF	chr8:121136580-121136730	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:121136560-121136710	HEEpiC	esophagus:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
32	CTCF	chr8:121136560-121136710	AG04449	skin:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
33	CTCF	chr8:121136560-121136710	AoAF	blood vessel:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
34	RAD21	chr8:121136556-121136733	K562	blood:	n/a	chr8:121136562-121136575 chr8:121136556-121136570
35	CTCF	chr8:121136566-121136675	Spleen_OC	spleen:	n/a	chr8:121136567-121136576
36	CTCF	chr8:121136580-121136730	HepG2	liver:	n/a	n/a
37	CTCF	chr8:121136580-121136730	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr8:121136520-121136670	NHEK	skin:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
39	CTCF	chr8:121136580-121136730	NHDF-neo	bronchial:	n/a	n/a
40	RAD21	chr8:121136433-121136900	ECC-1	luminal epithelium:	n/a	chr8:121136562-121136575 chr8:121136556-121136570
41	CTCF	chr8:121136520-121136670	WI-38	lung:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
42	RAD21	chr8:121136481-121136802	HepG2	liver:	n/a	chr8:121136562-121136575 chr8:121136556-121136570
43	CTCF	chr8:121136554-121136727	GM19240	blood:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
44	CTCF	chr8:121136580-121136730	HCT-116	colon:	n/a	n/a
45	CTCF	chr8:121136580-121136730	HAc	cerebellar:	n/a	n/a
46	CTCF	chr8:121136580-121136730	GM12872	blood:	n/a	n/a
47	CTCF	chr8:121136489-121136814	GM12878	blood:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576
48	CTCF	chr8:121136580-121136730	AG10803	skin:	n/a	n/a
49	CTCF	chr8:121136560-121136710	HCT-116	colon:	n/a	chr8:121136563-121136576 chr8:121136567-121136576
50	CTCF	chr8:121136448-121136802	H1-hESC	embryonic stem cell:	n/a	chr8:121136520-121136528 chr8:121136563-121136576 chr8:121136567-121136576

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:121136534-121136584	NB4	blood:	n/a
2	chr8:121136534-121136584	SK-N-SH	brain:	n/a
3	chr8:121136534-121136584	HepG2	liver:	n/a
4	chr8:121136534-121136584	NT2-D1	testis:	n/a
5	chr8:121136534-121136584	CMK	blood:	n/a
6	chr8:121136534-121136584	HCF	heart:	n/a
7	chr8:121136534-121136584	ovcar-3	ovarian:	n/a
8	chr8:121136534-121136584	IMR90	lung:	fetal
9	chr8:121136534-121136584	GM12891	blood:	n/a
10	chr8:121136534-121136584	AG04450	lung:	fetal
11	chr8:121136534-121136584	HIPEpiC	eye:	n/a
12	chr8:121136534-121136584	NH-A	brain:	n/a
13	chr8:121136534-121136584	GM06990	blood:	n/a
14	chr8:121136534-121136584	HL-60	blood:	n/a
15	chr8:121136534-121136584	PANC-1	pancreas:	n/a
16	chr8:121136534-121136584	LNCaP	prostate:	n/a
17	chr8:121136534-121136584	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:121136534-121136584	AoSMC	blood vessel:	n/a
19	chr8:121136534-121136584	Caco-2	colon:	n/a
20	chr8:121136534-121136584	H1-hESC	embryonic stem cell:	embryo
21	chr8:121136534-121136584	Hela-S3	cervix:	n/a
22	chr8:121136534-121136584	AG04449	skin:	fetal
23	chr8:121136534-121136584	HRPEpiC	eye:	n/a
24	chr8:121136534-121136584	A549	lung:	n/a
25	chr8:121136534-121136584	BJ	skin:	n/a
26	chr8:121136534-121136584	HCT-116	colon:	n/a
27	chr8:121136534-121136584	MCF-7	breast:	n/a
28	chr8:121136534-121136584	HRE	kidney:	n/a
29	chr8:121136534-121136584	GM19239	blood:	n/a
30	chr8:121136534-121136584	HCPEpiC	choroid plexus:	n/a
31	chr8:121136534-121136584	U87	brain:	n/a
32	chr8:121136534-121136584	SK-N-MC	brain:	n/a
33	chr8:121136534-121136584	RPTEC	kidney:	n/a
34	chr8:121136534-121136584	AG09309	skin:	n/a
35	chr8:121136534-121136584	K562	blood:	n/a
36	chr8:121136534-121136584	HNPCEpiC	eye:	n/a
37	chr8:121136534-121136584	HMEC	breast:	n/a
38	chr8:121136534-121136584	HEEpiC	esophagus:	n/a
39	chr8:121136534-121136584	BE2_C	brain:	n/a
40	chr8:121136534-121136584	AG10803	skin:	n/a
41	chr8:121136534-121136584	GM12892	blood:	n/a
42	chr8:121136534-121136584	GM12878	blood:	n/a
43	chr8:121136534-121136584	HRCEpiC	kidney:	n/a
44	chr8:121136534-121136584	MCF10A-Er-Src	breast:	n/a
45	chr8:121136534-121136584	Jurkat	blood:	n/a
46	chr8:121136534-121136584	HAEpiC	amniotic membrane:	n/a
47	chr8:121136534-121136584	PrEC	prostate:	n/a
48	chr8:121136534-121136584	ProgFib	skin:	n/a
49	chr8:121136534-121136584	Hepatocyte	liver:	n/a
50	chr8:121136534-121136584	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr8:121135175..121137414-chr8:121356303..121358717,45	MCF-7	breast:
2	chr8:121134772..121137578-chr8:121356736..121359144,3	MCF-7	breast:
3	chr8:121135918..121136601-chr8:121951029..121951928,2	K562	blood:
4	chr8:121135412..121137333-chr8:121357344..121358726,20	MCF-7	breast:
5	chr8:121135850..121136688-chr8:121433864..121434413,2	K562	blood:

Variant related genes	Relation type
COL14A1	TF binding region
COL14A1	CpG island
ENSG00000187955	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10086829	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10087151	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10096465	1.00[YRI][hapmap]
rs10104973	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10110722	1.00[CEU][hapmap];0.85[TSI][hapmap];0.87[EUR][1000 genomes]
rs10808507	0.86[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10955954	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11774123	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12543460	0.88[EUR][1000 genomes]
rs12548223	1.00[YRI][hapmap]
rs12678023	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1519814	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2326434	0.82[ASW][hapmap]
rs4133251	1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4271006	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4369033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4478617	1.00[CEU][hapmap]
rs4504680	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4588897	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4601361	0.95[CEU][hapmap];0.81[CHD][hapmap];0.85[TSI][hapmap];0.88[EUR][1000 genomes]
rs4871036	0.90[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4871037	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4871040	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4871045	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6469900	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6469901	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469902	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6983133	0.90[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6992410	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6995843	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7000103	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7000609	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7016388	0.90[CEU][hapmap];0.87[CHB][hapmap];0.83[CHD][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7818027	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7822384	1.00[ASW][hapmap];0.81[CHD][hapmap]
rs7826920	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7827008	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv3348294	chr8:121000288-121250984	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv6364	chr8:121107149-121152206	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4871041	MTBP	cis	cerebellum	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121135800-121136600	Flanking Active TSS	Adipose Nuclei	Adipose
2	chr8:121135800-121136600	Flanking Active TSS	Brain Hippocampus Middle	brain
3	chr8:121135800-121136600	Active TSS	Brain Substantia Nigra	brain
4	chr8:121135800-121136600	Flanking Active TSS	Stomach Smooth Muscle	stomach
5	chr8:121135800-121136600	Flanking Active TSS	Osteobl	bone
6	chr8:121135800-121136800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:121135800-121136800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:121135800-121136800	Bivalent/Poised TSS	Fetal Brain Female	brain
9	chr8:121135800-121137000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:121135800-121137000	Flanking Active TSS	Brain Anterior Caudate	brain
11	chr8:121135800-121137000	Enhancers	Pancreas	Pancrea
12	chr8:121135800-121137000	Active TSS	Right Ventricle	heart
13	chr8:121135800-121137200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:121135800-121137400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr8:121135800-121137400	Active TSS	Left Ventricle	heart
16	chr8:121135800-121137600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr8:121135800-121137600	Active TSS	Brain Angular Gyrus	brain
18	chr8:121135800-121137600	Active TSS	Right Atrium	heart
19	chr8:121135800-121137800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr8:121135800-121137800	Active TSS	Fetal Kidney	kidney
21	chr8:121135800-121137800	Enhancers	Spleen	Spleen
22	chr8:121136000-121136600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr8:121136000-121136600	Flanking Active TSS	Fetal Intestine Small	intestine
24	chr8:121136000-121136600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
25	chr8:121136000-121136600	Flanking Active TSS	Rectal Smooth Muscle	rectum
26	chr8:121136000-121136600	Flanking Active TSS	NHDF-Ad	bronchial
27	chr8:121136000-121136800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:121136000-121136800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
29	chr8:121136000-121136800	Flanking Bivalent TSS/Enh	Fetal Lung	lung
30	chr8:121136000-121137000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:121136000-121137000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:121136000-121137000	Enhancers	Esophagus	oesophagus
33	chr8:121136000-121137000	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr8:121136000-121137000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
35	chr8:121136000-121137000	Active TSS	HMEC	breast
36	chr8:121136000-121137200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
37	chr8:121136000-121137200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:121136000-121137200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:121136000-121137200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:121136000-121137200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
41	chr8:121136000-121137200	Flanking Active TSS	NH-A	brain
42	chr8:121136000-121137200	Flanking Active TSS	NHLF	lung
43	chr8:121136000-121137400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
44	chr8:121136000-121137600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr8:121136000-121137800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
46	chr8:121136000-121138000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:121136000-121138200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
48	chr8:121136000-121138200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr8:121136000-121138200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:121136000-121138200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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