Variant report

Variant	rs2074399
Chromosome Location	chr7:27282483-27282484
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
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	TCF7L2	chr7:27282055-27282655	PANC-1	pancreas:	n/a	chr7:27282285-27282294 chr7:27282282-27282296
2	CREB1	chr7:27282065-27282568	H1-hESC	embryonic stem cell:	n/a	n/a
3	CREB1	chr7:27282072-27282586	H1-hESC	embryonic stem cell:	n/a	n/a
4	SUZ12	chr7:27280823-27287156	NT2-D1	testis:	n/a	n/a
5	POLR2A	chr7:27281303-27282662	H1-neurons	neurons:	n/a	n/a
6	POLR2A	chr7:27281219-27282711	H1-neurons	neurons:	n/a	n/a
7	TCF7L2	chr7:27281947-27282603	HEK293	kidney:	n/a	chr7:27282285-27282294 chr7:27282282-27282296
8	SUZ12	chr7:27281809-27287391	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr7:27282140-27284056	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27282444-27282494	T-47D	breast:	n/a
2	chr7:27282444-27282494	BJ	skin:	n/a
3	chr7:27282444-27282494	BE2_C	brain:	n/a
4	chr7:27282444-27282494	HCPEpiC	choroid plexus:	n/a
5	chr7:27282444-27282494	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:27282444-27282494	H1-hESC	embryonic stem cell:	embryo
7	chr7:27282444-27282494	HCF	heart:	n/a
8	chr7:27282444-27282494	HIPEpiC	eye:	n/a
9	chr7:27282444-27282494	AG10803	skin:	n/a
10	chr7:27282444-27282494	K562	blood:	n/a
11	chr7:27282444-27282494	AG09309	skin:	n/a
12	chr7:27282444-27282494	ProgFib	skin:	n/a
13	chr7:27282444-27282494	NT2-D1	testis:	n/a
14	chr7:27282444-27282494	HRCEpiC	kidney:	n/a
15	chr7:27282444-27282494	CMK	blood:	n/a
16	chr7:27282444-27282494	A549	lung:	n/a
17	chr7:27282444-27282494	NHDF-neo	bronchial:	n/a
18	chr7:27282444-27282494	GM12891	blood:	n/a
19	chr7:27282444-27282494	HMEC	breast:	n/a
20	chr7:27282444-27282494	AoSMC	blood vessel:	n/a
21	chr7:27282444-27282494	GM12878	blood:	n/a
22	chr7:27282444-27282494	HEEpiC	esophagus:	n/a
23	chr7:27282444-27282494	HCT-116	colon:	n/a
24	chr7:27282444-27282494	MCF-7	breast:	n/a
25	chr7:27282444-27282494	Hela-S3	cervix:	n/a
26	chr7:27282444-27282494	ECC-1	luminal epithelium:	n/a
27	chr7:27282444-27282494	HAEpiC	amniotic membrane:	n/a
28	chr7:27282444-27282494	Jurkat	blood:	n/a
29	chr7:27282444-27282494	NHBE	bronchial:	n/a
30	chr7:27282444-27282494	HRPEpiC	eye:	n/a
31	chr7:27282444-27282494	NH-A	brain:	n/a
32	chr7:27282444-27282494	U87	brain:	n/a
33	chr7:27282444-27282494	RPTEC	kidney:	n/a
34	chr7:27282444-27282494	HL-60	blood:	n/a
35	chr7:27282444-27282494	SKMC	muscle:	n/a
36	chr7:27282444-27282494	HCM	heart:	n/a
37	chr7:27282444-27282494	Hepatocyte	liver:	n/a
38	chr7:27282444-27282494	SK-N-MC	brain:	n/a
39	chr7:27282444-27282494	AG09319	gingival:	n/a
40	chr7:27282444-27282494	HepG2	liver:	n/a
41	chr7:27282444-27282494	SAEC	small airway:	n/a
42	chr7:27282444-27282494	GM12892	blood:	n/a
43	chr7:27282444-27282494	SK-N-SH	brain:	n/a
44	chr7:27282444-27282494	SK-N-SH_RA	brain:	n/a
45	chr7:27282444-27282494	HNPCEpiC	eye:	n/a
46	chr7:27282444-27282494	PANC-1	pancreas:	n/a
47	chr7:27282444-27282494	GM19239	blood:	n/a
48	chr7:27282444-27282494	AG04450	lung:	fetal
49	chr7:27282444-27282494	ovcar-3	ovarian:	n/a
50	chr7:27282444-27282494	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:27230275-27238414..7:27282073-27287306	H1-hESC	embryonic stem cell:	embryo

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP1-170O19.17.1-2	chr7:27282087-27282581	ENSG00000253405.1

No data

Variant related genes	Relation type
EVX1	TF binding region
ENSG00000253308	TF binding region
EVX1	CpG island
ENSG00000253308	CpG island
ENSG00000106031	Chromatin interaction
ENSG00000243766	Chromatin interaction
ENSG00000253508	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10239543	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10262140	0.87[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs10264581	0.87[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs12666259	0.90[ASN][1000 genomes]
rs12700796	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13221828	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2158216	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2214412	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2391399	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2391402	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3801321	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4722677	0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs6461997	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6461998	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6461999	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6951104	0.81[ASN][1000 genomes]
rs6951180	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6956598	0.85[CEU][hapmap];0.92[GIH][hapmap];0.81[LWK][hapmap];0.90[MEX][hapmap];0.93[AMR][1000 genomes]
rs6960464	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6964896	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6973893	0.98[ASN][1000 genomes]
rs757179	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs757180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7782529	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 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	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
4	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
5	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
6	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
7	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
8	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
9	nsv1020608	chr7:27139892-27324004	Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
10	nsv538807	chr7:27139892-27324004	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers 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	182 gene(s)	inside rSNPs	diseases
11	nsv532118	chr7:27146920-27354205	Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv887879	chr7:27175295-27297791	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
13	esv1798853	chr7:27181568-27309266	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
14	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active 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	148 gene(s)	inside rSNPs	diseases
15	nsv887880	chr7:27205282-27294701	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
16	nsv887881	chr7:27205282-27297791	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
17	nsv887884	chr7:27206688-27297791	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
18	nsv1026327	chr7:27207777-27288521	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
19	nsv538808	chr7:27207777-27288521	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
20	nsv887886	chr7:27215041-27297791	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
21	nsv887889	chr7:27220831-27297791	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
22	nsv887892	chr7:27223563-27297791	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
23	nsv519583	chr7:27243962-27298264	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2074399	DFNA5	cis	parietal	SCAN
rs2074399	CRHR2	cis	parietal	SCAN

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27278400-27282800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:27278600-27282600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr7:27278800-27285000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:27280000-27285600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
5	chr7:27281800-27282600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
6	chr7:27281800-27283000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:27281800-27283200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
8	chr7:27281800-27283200	Bivalent Enhancer	Fetal Brain Male	brain
9	chr7:27282000-27282600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
10	chr7:27282000-27282600	Bivalent Enhancer	Fetal Heart	heart
11	chr7:27282000-27282600	Bivalent Enhancer	Fetal Thymus	thymus
12	chr7:27282000-27282600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
13	chr7:27282000-27282800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr7:27282000-27282800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr7:27282000-27282800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr7:27282000-27282800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
17	chr7:27282000-27282800	Bivalent Enhancer	Fetal Intestine Large	intestine
18	chr7:27282000-27282800	Flanking Bivalent TSS/Enh	Placenta	Placenta
19	chr7:27282000-27282800	Bivalent/Poised TSS	Osteobl	bone
20	chr7:27282000-27283000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
21	chr7:27282000-27283200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:27282000-27283200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
23	chr7:27282000-27283200	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:27282000-27283200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr7:27282000-27283200	Active TSS	Right Atrium	heart
26	chr7:27282000-27283400	Bivalent Enhancer	Fetal Stomach	stomach
27	chr7:27282000-27283400	Enhancers	Pancreas	Pancrea
28	chr7:27282000-27283400	Bivalent/Poised TSS	HSMM	muscle
29	chr7:27282000-27283600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr7:27282000-27283600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:27282000-27283600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:27282000-27285000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chr7:27282000-27285400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr7:27282200-27282600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
35	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
36	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:27282200-27282600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
39	chr7:27282200-27282600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
40	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:27282200-27282600	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
42	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Liver	Liver
43	chr7:27282200-27282600	Bivalent Enhancer	Brain Angular Gyrus	brain
44	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
45	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
46	chr7:27282200-27282600	Flanking Active TSS	Right Ventricle	heart
47	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
48	chr7:27282200-27282600	Flanking Bivalent TSS/Enh	HMEC	breast
49	chr7:27282200-27282600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
50	chr7:27282200-27282600	Bivalent/Poised TSS	NHEK	skin

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