Variant report

Variant	rs12291042
Chromosome Location	chr11:63683758-63683759
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	MAX	chr11:63683729-63684952	A549	lung:	n/a	n/a
2	POLR2A	chr11:63683697-63684279	H1-hESC	embryonic stem cell:	n/a	n/a
3	RAD21	chr11:63682620-63684442	SK-N-SH	brain:	n/a	chr11:63682798-63682808 chr11:63684308-63684321 chr11:63684016-63684035 chr11:63682798-63682810 chr11:63683940-63683953 chr11:63682796-63682809 chr11:63683756-63683766
4	YY1	chr11:63683709-63684199	K562	blood:	n/a	chr11:63683751-63683762
5	CTCF	chr11:63683737-63684224	K562	blood:	n/a	chr11:63683943-63683956 chr11:63684015-63684033
6	ZBTB7A	chr11:63683640-63684455	K562	blood:	n/a	chr11:63684246-63684254
7	RAD21	chr11:63683756-63684246	H1-hESC	embryonic stem cell:	n/a	chr11:63684016-63684035 chr11:63683940-63683953 chr11:63683756-63683766
8	CTCF	chr11:63683680-63683830	Hela-S3	cervix:	n/a	n/a
9	YY1	chr11:63683410-63684450	HepG2	liver:	n/a	chr11:63684190-63684201 chr11:63684423-63684437 chr11:63683751-63683762
10	POLR2A	chr11:63683377-63684284	H1-neurons	neurons:	n/a	n/a
11	POLR2A	chr11:63683302-63684289	MCF-7	breast:	n/a	n/a
12	SIN3AK20	chr11:63683696-63684470	PANC-1	pancreas:	n/a	n/a
13	MXI1	chr11:63682495-63686664	SK-N-SH	brain:	n/a	chr11:63684285-63684294
14	SMC3	chr11:63682501-63684951	SK-N-SH	brain:	n/a	chr11:63682772-63682779 chr11:63682956-63682966 chr11:63683582-63683592 chr11:63684771-63684785
15	POLR2A	chr11:63683525-63684412	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr11:63683757-63684194	PFSK-1	brain:	n/a	n/a
17	POLR2A	chr11:63683215-63684084	SK-N-MC	brain:	n/a	n/a
18	CTCF	chr11:63683320-63684922	SK-N-SH	brain:	n/a	chr11:63683943-63683956 chr11:63684856-63684865 chr11:63684015-63684033 chr11:63684772-63684781
19	RAD21	chr11:63683748-63684298	ECC-1	luminal epithelium:	n/a	chr11:63684016-63684035 chr11:63683940-63683953 chr11:63683756-63683766
20	BCL3	chr11:63683714-63684103	A549	lung:	n/a	n/a
21	MAX	chr11:63683639-63684233	H1-hESC	embryonic stem cell:	n/a	n/a
22	REST	chr11:63683413-63686259	H1-neurons	neurons:	n/a	chr11:63685888-63685898 chr11:63683931-63683944 chr11:63683635-63683648 chr11:63684423-63684436 chr11:63683688-63683701 chr11:63684253-63684266 chr11:63685102-63685115
23	ZBTB7A	chr11:63683691-63686037	ECC-1	luminal epithelium:	n/a	chr11:63684246-63684254
24	CTCF	chr11:63683727-63684246	H1-hESC	embryonic stem cell:	n/a	chr11:63683943-63683956 chr11:63684015-63684033
25	POLR2A	chr11:63683743-63684225	HCT-116	colon:	n/a	n/a
26	RAD21	chr11:63683722-63684314	H1-hESC	embryonic stem cell:	n/a	chr11:63684016-63684035 chr11:63683940-63683953 chr11:63683756-63683766
27	CTCF	chr11:63683749-63684763	A549	lung:	n/a	chr11:63683943-63683956 chr11:63684015-63684033
28	MAZ	chr11:63683620-63685977	IMR90	lung:	n/a	chr11:63685552-63685561 chr11:63685551-63685561 chr11:63685594-63685604 chr11:63685582-63685592 chr11:63685551-63685562 chr11:63685551-63685562
29	SIN3A	chr11:63683280-63686060	H1-hESC	embryonic stem cell:	n/a	chr11:63683937-63683950 chr11:63683933-63683944 chr11:63683931-63683944 chr11:63684423-63684436 chr11:63684305-63684316
30	SIN3AK20	chr11:63683665-63684248	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:63683701-63684307	H1-hESC	embryonic stem cell:	n/a	n/a
32	YY1	chr11:63683696-63684248	H1-hESC	embryonic stem cell:	n/a	chr11:63684190-63684201 chr11:63683751-63683762
33	CTCF	chr11:63683627-63684343	K562	blood:	n/a	chr11:63683943-63683956 chr11:63684015-63684033
34	TCF12	chr11:63683719-63684216	ECC-1	luminal epithelium:	n/a	chr11:63683937-63683947
35	POLR2A	chr11:63683185-63684938	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:63683464-63684251	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63683744-63683794	U87	brain:	n/a
2	chr11:63683744-63683794	GM12892	blood:	n/a
3	chr11:63683744-63683794	HRPEpiC	eye:	n/a
4	chr11:63683744-63683794	ECC-1	luminal epithelium:	n/a
5	chr11:63683744-63683794	A549	lung:	n/a
6	chr11:63683744-63683794	PrEC	prostate:	n/a
7	chr11:63683744-63683794	NB4	blood:	n/a
8	chr11:63683744-63683794	MCF10A-Er-Src	breast:	n/a
9	chr11:63683744-63683794	PANC-1	pancreas:	n/a
10	chr11:63683744-63683794	IMR90	lung:	fetal
11	chr11:63683744-63683794	HL-60	blood:	n/a
12	chr11:63683744-63683794	HEEpiC	esophagus:	n/a
13	chr11:63683744-63683794	RPTEC	kidney:	n/a
14	chr11:63683744-63683794	HMEC	breast:	n/a
15	chr11:63683744-63683794	LNCaP	prostate:	n/a
16	chr11:63683744-63683794	HIPEpiC	eye:	n/a
17	chr11:63683744-63683794	AG09319	gingival:	n/a
18	chr11:63683744-63683794	BJ	skin:	n/a
19	chr11:63683744-63683794	AG10803	skin:	n/a
20	chr11:63683744-63683794	SK-N-SH	brain:	n/a
21	chr11:63683744-63683794	T-47D	breast:	n/a
22	chr11:63683744-63683794	HRE	kidney:	n/a
23	chr11:63683744-63683794	SAEC	small airway:	n/a
24	chr11:63683744-63683794	HCPEpiC	choroid plexus:	n/a
25	chr11:63683744-63683794	HNPCEpiC	eye:	n/a
26	chr11:63683744-63683794	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:63683744-63683794	Jurkat	blood:	n/a
28	chr11:63683744-63683794	SK-N-SH_RA	brain:	n/a
29	chr11:63683744-63683794	NT2-D1	testis:	n/a
30	chr11:63683744-63683794	AG04450	lung:	fetal
31	chr11:63683744-63683794	HEK293	kidney:	embryo
32	chr11:63683744-63683794	AG09309	skin:	n/a
33	chr11:63683744-63683794	ovcar-3	ovarian:	n/a
34	chr11:63683744-63683794	GM12891	blood:	n/a
35	chr11:63683744-63683794	Caco-2	colon:	n/a
36	chr11:63683744-63683794	MCF-7	breast:	n/a
37	chr11:63683744-63683794	NHDF-neo	bronchial:	n/a
38	chr11:63683744-63683794	H1-hESC	embryonic stem cell:	embryo
39	chr11:63683744-63683794	GM06990	blood:	n/a
40	chr11:63683744-63683794	GM12878	blood:	n/a
41	chr11:63683744-63683794	NH-A	brain:	n/a
42	chr11:63683744-63683794	NHBE	bronchial:	n/a
43	chr11:63683744-63683794	AoSMC	blood vessel:	n/a
44	chr11:63683744-63683794	BE2_C	brain:	n/a
45	chr11:63683744-63683794	HCF	heart:	n/a
46	chr11:63683744-63683794	SK-N-MC	brain:	n/a
47	chr11:63683744-63683794	HCM	heart:	n/a
48	chr11:63683744-63683794	PFSK-1	brain:	n/a
49	chr11:63683744-63683794	HCT-116	colon:	n/a
50	chr11:63683744-63683794	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63683405..63684071-chr11:63712749..63713693,2	MCF-7	breast:
2	chr11:63683018..63687693-chr11:63704987..63708969,9	MCF-7	breast:
3	chr11:63683426..63687637-chr11:63739381..63744575,6	K562	blood:
4	chr11:63674570..63680304-chr11:63681753..63686803,9	MCF-7	breast:
5	chr11:63682847..63685544-chr11:63752668..63755278,2	MCF-7	breast:
6	chr11:63535779..63536323-chr11:63683262..63684232,2	MCF-7	breast:
7	chr11:63604824..63606885-chr11:63683071..63686195,3	K562	blood:
8	chr11:63605631..63608231-chr11:63683000..63685015,3	MCF-7	breast:
9	chr11:63682437..63684177-chr8:101963345..101965664,2	MCF-7	breast:
10	chr11:63682343..63688338-chr11:63931257..63935493,5	K562	blood:
11	chr11:63666544..63671236-chr11:63682476..63685803,4	MCF-7	breast:
12	chr11:63673944..63681438-chr11:63681488..63685981,13	K562	blood:
13	chr11:63579193..63582428-chr11:63682051..63685961,4	K562	blood:
14	chr11:63682242..63690244-chr11:63703955..63713214,18	K562	blood:
15	chr11:63683456..63690158-chr11:63704393..63714412,17	K562	blood:
16	chr11:63605131..63609420-chr11:63682910..63687369,4	MCF-7	breast:
17	chr11:63683295..63687930-chr11:63703819..63708534,6	MCF-7	breast:
18	chr11:63580176..63582428-chr11:63682563..63684680,2	K562	blood:

Variant related genes	Relation type
RCOR2	TF binding region
RCOR2	CpG island
ENSG00000164924	Chromatin interaction
ENSG00000072518	Chromatin interaction
ENSG00000167771	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000167770	Chromatin interaction
ENSG00000255651	Chromatin interaction
ENSG00000168005	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000256100	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10897460	1.00[EUR][1000 genomes]
rs11231632	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11231634	1.00[EUR][1000 genomes]
rs11494059	0.96[AFR][1000 genomes]
rs12099085	1.00[EUR][1000 genomes]
rs12271959	1.00[EUR][1000 genomes]
rs12277386	1.00[EUR][1000 genomes]
rs12277838	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12288290	1.00[EUR][1000 genomes]
rs12295918	1.00[EUR][1000 genomes]
rs13377315	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs320110	1.00[EUR][1000 genomes]
rs57219930	1.00[EUR][1000 genomes]
rs57864399	1.00[EUR][1000 genomes]
rs58678024	1.00[EUR][1000 genomes]
rs59423787	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59642000	1.00[EUR][1000 genomes]
rs60107756	1.00[EUR][1000 genomes]
rs61475860	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7110433	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7929867	1.00[EUR][1000 genomes]
rs7933899	1.00[EUR][1000 genomes]
rs7948681	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7952003	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9630214	1.00[EUR][1000 genomes]
rs9630215	1.00[EUR][1000 genomes]
rs9888136	1.00[EUR][1000 genomes]
rs9888177	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
9	nsv897632	chr11:63670787-63688693	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv897633	chr11:63670787-63691049	Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv897634	chr11:63670787-63698538	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv897635	chr11:63674926-63688693	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv897636	chr11:63676067-63688693	Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv897637	chr11:63676067-63691049	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
15	nsv897638	chr11:63676562-63688693	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	14 gene(s)	inside rSNPs	diseases
16	esv3378640	chr11:63683601-63686149	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63671000-63683800	Weak transcription	NHDF-Ad	bronchial
2	chr11:63672400-63683800	Weak transcription	Psoas Muscle	Psoas
3	chr11:63676600-63684000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:63676600-63684000	Weak transcription	Aorta	Aorta
5	chr11:63679200-63684000	Weak transcription	HSMMtube	muscle
6	chr11:63682600-63683800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr11:63682600-63683800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr11:63682600-63683800	Enhancers	Adipose Nuclei	Adipose
9	chr11:63682600-63683800	Enhancers	Esophagus	oesophagus
10	chr11:63682600-63683800	Enhancers	Placenta	Placenta
11	chr11:63682600-63683800	Enhancers	Left Ventricle	heart
12	chr11:63682600-63684000	Enhancers	Gastric	stomach
13	chr11:63682600-63684200	Enhancers	Lung	lung
14	chr11:63682600-63684200	Bivalent Enhancer	Stomach Mucosa	stomach
15	chr11:63682600-63685800	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr11:63682600-63688800	Active TSS	H9 Cell Line	embryonic stem cell
17	chr11:63682800-63683800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
18	chr11:63682800-63684000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr11:63682800-63684400	Bivalent Enhancer	Spleen	Spleen
20	chr11:63682800-63685000	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr11:63682800-63685200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr11:63682800-63685200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:63682800-63685800	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr11:63682800-63687400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:63683000-63685000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:63683000-63685000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:63683000-63685600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:63683000-63685800	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr11:63683000-63686000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr11:63683000-63686000	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr11:63683000-63686000	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr11:63683000-63687200	Active TSS	H1 Cell Line	embryonic stem cell
33	chr11:63683200-63683800	Enhancers	Primary B cells from cord blood	blood
34	chr11:63683200-63683800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:63683200-63683800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:63683200-63683800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr11:63683200-63683800	Enhancers	Duodenum Mucosa	Duodenum
38	chr11:63683200-63683800	Enhancers	Small Intestine	intestine
39	chr11:63683200-63683800	Active TSS	NHLF	lung
40	chr11:63683200-63684000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
41	chr11:63683200-63684200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr11:63683200-63684200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:63683200-63684200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:63683200-63684200	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr11:63683200-63684200	Flanking Active TSS	Fetal Lung	lung
46	chr11:63683200-63684200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr11:63683200-63684400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:63683200-63684400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:63683200-63684400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:63683200-63684400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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