Variant report

Variant	rs4151667
Chromosome Location	chr6:31914024-31914025
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31913398-31914808	HepG2	liver:	n/a	n/a
2	STAT3	chr6:31913142-31914047	MCF10A-Er-Src	breast:	n/a	chr6:31913730-31913741 chr6:31913492-31913504 chr6:31913778-31913789 chr6:31913494-31913506
3	POLR2A	chr6:31913170-31914079	Hela-S3	cervix:	n/a	n/a
4	ELF1	chr6:31913099-31914148	HepG2	liver:	n/a	n/a
5	HNF4A	chr6:31913191-31914290	HepG2	liver:	n/a	chr6:31913566-31913579 chr6:31913565-31913580 chr6:31913565-31913580 chr6:31913567-31913579 chr6:31913567-31913579 chr6:31913565-31913580 chr6:31913565-31913580
6	TCF7L2	chr6:31914015-31914448	PANC-1	pancreas:	n/a	n/a
7	HEY1	chr6:31913342-31914128	HepG2	liver:	n/a	n/a
8	POLR2A	chr6:31913175-31914144	U87	brain:	n/a	n/a
9	POLR2A	chr6:31913284-31915077	HepG2	liver:	n/a	n/a
10	JUND	chr6:31913321-31914130	HepG2	liver:	n/a	n/a
11	SIN3AK20	chr6:31913420-31914060	HepG2	liver:	n/a	n/a
12	USF2	chr6:31913853-31914051	HepG2	liver:	n/a	n/a
13	PBX3	chr6:31913211-31914050	SK-N-SH	brain:	n/a	n/a
14	POLR2A	chr6:31913188-31914168	Hela-S3	cervix:	n/a	n/a
15	MAZ	chr6:31913250-31914083	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr6:31913316-31914139	HepG2	liver:	n/a	n/a
17	MYBL2	chr6:31912952-31914524	HepG2	liver:	n/a	n/a
18	POLR2A	chr6:31913104-31914326	MCF10A-Er-Src	breast:	n/a	n/a
19	STAT3	chr6:31913150-31914301	MCF10A-Er-Src	breast:	n/a	chr6:31913730-31913741 chr6:31913492-31913504 chr6:31913778-31913789 chr6:31913494-31913506
20	MAZ	chr6:31913000-31914124	IMR90	lung:	n/a	n/a
21	RAD21	chr6:31913427-31914106	HepG2	liver:	n/a	n/a
22	POLR2A	chr6:31913808-31914209	H1-neurons	neurons:	n/a	n/a
23	NFIC	chr6:31913113-31914180	HepG2	liver:	n/a	n/a
24	POLR2A	chr6:31913302-31914527	HepG2	liver:	n/a	n/a
25	TBP	chr6:31913362-31914086	HepG2	liver:	n/a	n/a
26	MBD4	chr6:31913137-31914605	HepG2	liver:	n/a	n/a
27	NFIC	chr6:31913121-31914204	HepG2	liver:	n/a	n/a
28	POLR2A	chr6:31913398-31914133	HepG2	liver:	n/a	n/a
29	MXI1	chr6:31913126-31914112	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:31913316-31914396	HepG2	liver:	n/a	n/a
31	RAD21	chr6:31913311-31914070	HepG2	liver:	n/a	n/a
32	POLR2A	chr6:31913107-31918251	MCF10A-Er-Src	breast:	n/a	n/a
33	HNF4G	chr6:31913239-31914345	HepG2	liver:	n/a	chr6:31913566-31913579 chr6:31913565-31913580 chr6:31913565-31913580 chr6:31913567-31913579 chr6:31913567-31913579 chr6:31913565-31913580
34	FOXA1	chr6:31913046-31914037	HepG2	liver:	n/a	n/a
35	TCF7L2	chr6:31913220-31914456	Hela-S3	cervix:	n/a	n/a
36	FOXA1	chr6:31913158-31914030	HepG2	liver:	n/a	n/a
37	POLR2A	chr6:31913128-31914133	Hela-S3	cervix:	n/a	n/a
38	TAF1	chr6:31913707-31914146	HepG2	liver:	n/a	n/a
39	MYBL2	chr6:31913068-31914412	HepG2	liver:	n/a	n/a
40	FOXA2	chr6:31913127-31914435	HepG2	liver:	n/a	n/a
41	YY1	chr6:31912908-31914121	HepG2	liver:	n/a	n/a
42	FOSL2	chr6:31913178-31914144	HepG2	liver:	n/a	n/a
43	EP300	chr6:31913305-31914076	HepG2	liver:	n/a	n/a
44	SP1	chr6:31913148-31914155	HepG2	liver:	n/a	chr6:31913488-31913502 chr6:31913492-31913501
45	REST	chr6:31913196-31914095	HepG2	liver:	n/a	n/a
46	TCF7L2	chr6:31913950-31914447	HepG2	liver:	n/a	n/a
47	SMARCC1	chr6:31913193-31914108	Hela-S3	cervix:	n/a	n/a
48	RCOR1	chr6:31913173-31914208	HepG2	liver:	n/a	n/a
49	CEBPD	chr6:31913288-31914121	HepG2	liver:	n/a	n/a
50	POLR2A	chr6:31912538-31923721	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31913995-31914045	AoSMC	blood vessel:	n/a
2	chr6:31913995-31914045	HCF	heart:	n/a
3	chr6:31913995-31914045	GM12892	blood:	n/a
4	chr6:31913995-31914045	ECC-1	luminal epithelium:	n/a
5	chr6:31913995-31914045	HUVEC	blood vessel:	n/a
6	chr6:31913995-31914045	A549	lung:	n/a
7	chr6:31913995-31914045	IMR90	lung:	fetal
8	chr6:31913995-31914045	HMEC	breast:	n/a
9	chr6:31913995-31914045	PrEC	prostate:	n/a
10	chr6:31913995-31914045	GM12891	blood:	n/a
11	chr6:31913995-31914045	Jurkat	blood:	n/a
12	chr6:31913995-31914045	AG04450	lung:	fetal
13	chr6:31913995-31914045	Caco-2	colon:	n/a
14	chr6:31913995-31914045	CMK	blood:	n/a
15	chr6:31913995-31914045	U87	brain:	n/a
16	chr6:31913995-31914045	BE2_C	brain:	n/a
17	chr6:31913995-31914045	NHBE	bronchial:	n/a
18	chr6:31913995-31914045	SAEC	small airway:	n/a
19	chr6:31913995-31914045	HEEpiC	esophagus:	n/a
20	chr6:31913995-31914045	Hepatocyte	liver:	n/a
21	chr6:31913995-31914045	HCPEpiC	choroid plexus:	n/a
22	chr6:31913995-31914045	SK-N-SH	brain:	n/a
23	chr6:31913995-31914045	HL-60	blood:	n/a
24	chr6:31913995-31914045	Hela-S3	cervix:	n/a
25	chr6:31913995-31914045	AG10803	skin:	n/a
26	chr6:31913995-31914045	BJ	skin:	n/a
27	chr6:31913995-31914045	GM06990	blood:	n/a
28	chr6:31913995-31914045	NHDF-neo	bronchial:	n/a
29	chr6:31913995-31914045	AG04449	skin:	fetal
30	chr6:31913995-31914045	GM19239	blood:	n/a
31	chr6:31913995-31914045	HRE	kidney:	n/a
32	chr6:31913995-31914045	SK-N-SH_RA	brain:	n/a
33	chr6:31913995-31914045	HNPCEpiC	eye:	n/a
34	chr6:31913995-31914045	MCF10A-Er-Src	breast:	n/a
35	chr6:31913995-31914045	NB4	blood:	n/a
36	chr6:31913995-31914045	RPTEC	kidney:	n/a
37	chr6:31913995-31914045	AG09319	gingival:	n/a
38	chr6:31913995-31914045	HepG2	liver:	n/a
39	chr6:31913995-31914045	GM12878	blood:	n/a
40	chr6:31913995-31914045	HRCEpiC	kidney:	n/a
41	chr6:31913995-31914045	HEK293	kidney:	embryo
42	chr6:31913995-31914045	HAEpiC	amniotic membrane:	n/a
43	chr6:31913995-31914045	ProgFib	skin:	n/a
44	chr6:31913995-31914045	LNCaP	prostate:	n/a
45	chr6:31913995-31914045	K562	blood:	n/a
46	chr6:31913995-31914045	HCM	heart:	n/a
47	chr6:31913995-31914045	MCF-7	breast:	n/a
48	chr6:31913995-31914045	T-47D	breast:	n/a
49	chr6:31913995-31914045	AG09309	skin:	n/a
50	chr6:31913995-31914045	NT2-D1	testis:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31828952..31831553-chr6:31912715..31914981,2	K562	blood:
2	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
3	chr6:31854115..31856826-chr6:31913867..31915528,2	MCF-7	breast:
4	chr6:31911295..31914045-chr6:32938834..32940985,2	MCF-7	breast:
5	chr6:31893919..31897907-chr6:31913762..31916831,4	MCF-7	breast:
6	chr6:31792517..31796452-chr6:31911867..31914768,3	MCF-7	breast:
7	chr6:31802757..31805057-chr6:31913533..31915744,2	MCF-7	breast:
8	chr6:31868502..31871158-chr6:31911705..31915017,4	MCF-7	breast:
9	chr6:31830894..31832674-chr6:31912375..31914374,2	MCF-7	breast:
10	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
11	chr6:31701400..31704942-chr6:31911756..31915207,3	MCF-7	breast:

No data

Variant related genes	Relation type
CFB	TF binding region
CFB	CpG island
ENSG00000204371	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204387	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17201417	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs17201560	0.87[AMR][1000 genomes]
rs17207748	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs41270464	0.86[AFR][1000 genomes]
rs4151671	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4151672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9332739	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9332741	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
11	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' 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	197 gene(s)	inside rSNPs	diseases
12	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
13	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
14	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884512	chr6:31908470-31933161	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4151667	DOM3Z	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31908200-31918600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:31908800-31919400	Weak transcription	Ovary	ovary
3	chr6:31909200-31918800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr6:31912600-31914200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:31912600-31914400	Enhancers	Colon Smooth Muscle	Colon
6	chr6:31912600-31914400	Enhancers	Spleen	Spleen
7	chr6:31912600-31914800	Enhancers	Fetal Thymus	thymus
8	chr6:31912600-31915200	Enhancers	Esophagus	oesophagus
9	chr6:31912600-31915200	Flanking Active TSS	Hela-S3	cervix
10	chr6:31912800-31914200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:31912800-31914200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:31912800-31914400	Enhancers	Placenta Amnion	Placenta Amnion
13	chr6:31912800-31914400	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr6:31913000-31914200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:31913000-31914200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:31913000-31914200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr6:31913000-31914200	Enhancers	Lung	lung
18	chr6:31913000-31914200	Enhancers	HSMM	muscle
19	chr6:31913000-31914200	Flanking Active TSS	NHEK	skin
20	chr6:31913000-31914200	Flanking Active TSS	NHLF	lung
21	chr6:31913000-31914200	Flanking Active TSS	Osteobl	bone
22	chr6:31913000-31914400	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr6:31913000-31914600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:31913000-31914600	Flanking Active TSS	Colonic Mucosa	Colon
25	chr6:31913000-31918600	Weak transcription	Brain Hippocampus Middle	brain
26	chr6:31913200-31914200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:31913200-31914200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:31913200-31914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:31913200-31914200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:31913200-31914200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:31913200-31914200	Flanking Active TSS	NHDF-Ad	bronchial
32	chr6:31913200-31914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:31913200-31914400	Flanking Active TSS	Fetal Intestine Small	intestine
34	chr6:31913200-31914400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr6:31913200-31920800	Weak transcription	Small Intestine	intestine
36	chr6:31913400-31914200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:31913400-31914200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:31913400-31914200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr6:31913400-31914200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
40	chr6:31913400-31914200	Enhancers	HUVEC	blood vessel
41	chr6:31913400-31914400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr6:31913400-31914600	Active TSS	Brain Anterior Caudate	brain
43	chr6:31913400-31914800	Active TSS	Liver	Liver
44	chr6:31913400-31914800	Active TSS	Brain Substantia Nigra	brain
45	chr6:31913600-31914200	Enhancers	Placenta	Placenta
46	chr6:31913600-31914200	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr6:31913600-31914200	Enhancers	HSMMtube	muscle
48	chr6:31913600-31914400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr6:31913600-31917800	Weak transcription	A549	lung
50	chr6:31913600-31918600	Weak transcription	Brain Angular Gyrus	brain

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