Variant report

Variant	rs6668
Chromosome Location	chr7:27138183-27138184
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:27138140-27138290	HRE	kidney:	n/a	n/a
2	CTCF	chr7:27138040-27138190	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr7:27138107-27138255	NHEK	skin:	n/a	n/a
4	POLR2A	chr7:27137687-27138390	A549	lung:	n/a	n/a
5	CTCF	chr7:27138090-27138266	Fibrobl	skin:	n/a	n/a
6	SIN3AK20	chr7:27137647-27139006	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr7:27137961-27138799	MCF10A-Er-Src	breast:	n/a	n/a
8	CTCF	chr7:27138080-27138230	SAEC	small airway:	n/a	n/a
9	POLR2A	chr7:27137526-27139036	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr7:27138060-27138210	AG10803	skin:	n/a	n/a
11	CTCF	chr7:27138060-27138210	RPTEC	kidney:	n/a	n/a
12	TCF7L2	chr7:27137605-27139062	PANC-1	pancreas:	n/a	n/a
13	CTCF	chr7:27138160-27138310	NHEK	skin:	n/a	n/a
14	CTBP2	chr7:27137585-27138416	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr7:27138103-27139000	HUVEC	blood vessel:	n/a	n/a
16	RAD21	chr7:27137672-27138381	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr7:27135166-27139184	PANC-1	pancreas:	n/a	n/a
18	CTCF	chr7:27138160-27138310	GM12874	blood:	n/a	n/a
19	CTCF	chr7:27138060-27138210	HRE	kidney:	n/a	n/a
20	CTCF	chr7:27138100-27138250	HMF	breast:	n/a	n/a
21	CTCF	chr7:27138166-27138212	IMR90	lung:	n/a	n/a
22	POLR2A	chr7:27135394-27139167	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr7:27137292-27139236	PANC-1	pancreas:	n/a	n/a
24	CTCF	chr7:27138111-27138246	Gliobla	brain:	n/a	n/a
25	RAD21	chr7:27138063-27138229	SK-N-SH_RA	brain:	n/a	n/a
26	ZNF263	chr7:27135473-27138390	HEK293-T-REx	kidney:	n/a	chr7:27136937-27136946
27	CTCF	chr7:27138100-27138250	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr7:27138100-27138250	AG04449	skin:	n/a	n/a
29	CTCF	chr7:27138100-27138250	AG10803	skin:	n/a	n/a
30	POLR2A	chr7:27135386-27149832	IMR90	lung:	n/a	n/a
31	CTCF	chr7:27138120-27138270	GM12869	blood:	n/a	n/a
32	RAD21	chr7:27137895-27138344	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:27138080-27138230	NHLF	lung:	n/a	n/a
34	CTCF	chr7:27138120-27138270	GM12874	blood:	n/a	n/a
35	CTCF	chr7:27138080-27138230	HUVEC	blood vessel:	n/a	n/a
36	RAD21	chr7:27138008-27138336	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr7:27135269-27138922	IMR90	lung:	n/a	n/a
38	SUZ12	chr7:27137564-27139059	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr7:27134717-27152399	IMR90	lung:	n/a	chr7:27141647-27141657
40	CTCF	chr7:27138100-27138250	HPF	lung:	n/a	n/a
41	CTCF	chr7:27138120-27138270	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27138173-27138223	HL-60	blood:	n/a
2	chr7:27138173-27138223	GM06990	blood:	n/a
3	chr7:27138173-27138223	AoSMC	blood vessel:	n/a
4	chr7:27138173-27138223	MCF10A-Er-Src	breast:	n/a
5	chr7:27138173-27138223	Hela-S3	cervix:	n/a
6	chr7:27138173-27138223	HRE	kidney:	n/a
7	chr7:27138173-27138223	HEEpiC	esophagus:	n/a
8	chr7:27138173-27138223	AG04450	lung:	fetal
9	chr7:27138173-27138223	AG10803	skin:	n/a
10	chr7:27138173-27138223	NHBE	bronchial:	n/a
11	chr7:27138173-27138223	HCF	heart:	n/a
12	chr7:27138173-27138223	NB4	blood:	n/a
13	chr7:27138173-27138223	HepG2	liver:	n/a
14	chr7:27138173-27138223	HNPCEpiC	eye:	n/a
15	chr7:27138173-27138223	ProgFib	skin:	n/a
16	chr7:27138173-27138223	RPTEC	kidney:	n/a
17	chr7:27138173-27138223	HCT-116	colon:	n/a
18	chr7:27138173-27138223	Hepatocyte	liver:	n/a
19	chr7:27138173-27138223	ECC-1	luminal epithelium:	n/a
20	chr7:27138173-27138223	PFSK-1	brain:	n/a
21	chr7:27138173-27138223	NH-A	brain:	n/a
22	chr7:27138173-27138223	AG04449	skin:	fetal
23	chr7:27138173-27138223	H1-hESC	embryonic stem cell:	embryo
24	chr7:27138173-27138223	HUVEC	blood vessel:	n/a
25	chr7:27138173-27138223	Jurkat	blood:	n/a
26	chr7:27138173-27138223	BJ	skin:	n/a
27	chr7:27138173-27138223	BE2_C	brain:	n/a
28	chr7:27138173-27138223	T-47D	breast:	n/a
29	chr7:27138173-27138223	HCPEpiC	choroid plexus:	n/a
30	chr7:27138173-27138223	AG09319	gingival:	n/a
31	chr7:27138173-27138223	Caco-2	colon:	n/a
32	chr7:27138173-27138223	U87	brain:	n/a
33	chr7:27138173-27138223	AG09309	skin:	n/a
34	chr7:27138173-27138223	HIPEpiC	eye:	n/a
35	chr7:27138173-27138223	IMR90	lung:	fetal
36	chr7:27138173-27138223	PrEC	prostate:	n/a
37	chr7:27138173-27138223	SAEC	small airway:	n/a
38	chr7:27138173-27138223	CMK	blood:	n/a
39	chr7:27138173-27138223	PANC-1	pancreas:	n/a
40	chr7:27138173-27138223	GM19239	blood:	n/a
41	chr7:27138173-27138223	GM12878	blood:	n/a
42	chr7:27138173-27138223	HAEpiC	amniotic membrane:	n/a
43	chr7:27138173-27138223	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:27138173-27138223	HRCEpiC	kidney:	n/a
45	chr7:27138173-27138223	SKMC	muscle:	n/a
46	chr7:27138173-27138223	GM12891	blood:	n/a
47	chr7:27138173-27138223	SK-N-SH_RA	brain:	n/a
48	chr7:27138173-27138223	HCM	heart:	n/a
49	chr7:27138173-27138223	SK-N-SH	brain:	n/a
50	chr7:27138173-27138223	K562	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27136545..27139680-chr7:27140711..27142949,3	K562	blood:
2	chr12:53273583..53274199-chr7:27137731..27138330,2	MCF-7	breast:
3	7:27137201-27143270..7:27162022-27164727	H1-hESC	embryonic stem cell:	embryo
4	chr7:27136703..27139680-chr7:27141228..27142949,2	K562	blood:

No data

Variant related genes	Relation type
HOXA1	TF binding region
HOTAIRM1	TF binding region
HOXA1	CpG island
HOTAIRM1	CpG island
ENSG00000253552	Chromatin interaction
ENSG00000105996	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2522825	0.81[ASN][1000 genomes]
rs2712234	0.81[ASN][1000 genomes]
rs2712248	0.81[ASN][1000 genomes]
rs34725546	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
4	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv887856	chr7:27073731-27297791	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
6	nsv824038	chr7:27119294-27284522	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
7	nsv887857	chr7:27120689-27229549	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv824039	chr7:27121825-27294951	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
9	nsv824040	chr7:27121870-27295010	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
10	nsv887858	chr7:27127231-27188659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
11	nsv887860	chr7:27127231-27196069	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv887859	chr7:27127231-27196113	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv887861	chr7:27127231-27206688	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
14	nsv887862	chr7:27127231-27217359	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
15	nsv887863	chr7:27127231-27243106	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
16	nsv887864	chr7:27127231-27243962	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
17	nsv887865	chr7:27127231-27247279	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
18	nsv887866	chr7:27127231-27248373	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
19	nsv887867	chr7:27127231-27252246	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
20	nsv824041	chr7:27128039-27294951	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
21	nsv606463	chr7:27135314-27182245	Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
22	nsv887868	chr7:27135314-27202289	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
23	nsv887869	chr7:27135314-27297791	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
24	nsv887870	chr7:27136308-27154737	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
25	nsv887871	chr7:27136308-27179814	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
26	nsv887872	chr7:27136308-27181437	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
27	nsv887873	chr7:27136308-27186495	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
28	nsv887874	chr7:27136308-27196069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27134400-27139000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:27134400-27139000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:27134400-27139000	Active TSS	HMEC	breast
4	chr7:27134800-27138800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:27134800-27139200	Bivalent/Poised TSS	NH-A	brain
6	chr7:27134800-27140200	Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr7:27135000-27139400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr7:27135200-27138600	Active TSS	NHLF	lung
9	chr7:27135200-27139000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr7:27135200-27139200	Active TSS	Aorta	Aorta
11	chr7:27135200-27139200	Active TSS	Right Atrium	heart
12	chr7:27135400-27139000	Active TSS	Esophagus	oesophagus
13	chr7:27136200-27138400	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
14	chr7:27136200-27139200	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr7:27136400-27138600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
16	chr7:27136600-27138600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:27136600-27138800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:27136800-27138400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
19	chr7:27136800-27138600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr7:27136800-27138800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:27136800-27139000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
22	chr7:27136800-27139400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr7:27137000-27138200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:27137000-27138200	Flanking Active TSS	Colonic Mucosa	Colon
25	chr7:27137000-27138200	Enhancers	Spleen	Spleen
26	chr7:27137000-27138600	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr7:27137000-27138600	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr7:27137000-27138600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
29	chr7:27137000-27138800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
30	chr7:27137000-27139000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr7:27137000-27139000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr7:27137000-27139000	Enhancers	Pancreas	Pancrea
33	chr7:27137000-27146800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:27137200-27138200	Bivalent Enhancer	Primary T cells from cord blood	blood
35	chr7:27137200-27138200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:27137200-27138200	Bivalent/Poised TSS	Thymus	Thymus
37	chr7:27137200-27138400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
38	chr7:27137200-27138400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
39	chr7:27137200-27138400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr7:27137200-27138600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
41	chr7:27137200-27138600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr7:27137200-27138800	Active TSS	Psoas Muscle	Psoas
43	chr7:27137200-27139000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
44	chr7:27137200-27139600	Bivalent/Poised TSS	Fetal Lung	lung
45	chr7:27137400-27138200	Bivalent/Poised TSS	Liver	Liver
46	chr7:27137400-27138200	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr7:27137400-27138800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:27137400-27138800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
49	chr7:27137400-27139800	Flanking Active TSS	HUVEC	blood vessel
50	chr7:27137400-27140600	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links