Variant report

Variant	rs34797487
Chromosome Location	chr3:50230576-50230577
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr3:50229832-50230669	HCT-116	colon:	n/a	n/a
2	CTCF	chr3:50229874-50230590	A549	lung:	n/a	chr3:50230513-50230526
3	CTCF	chr3:50230560-50230710	K562	blood:	n/a	n/a
4	CTCF	chr3:50230500-50230650	NB4	blood:	n/a	chr3:50230513-50230526
5	CTCF	chr3:50230480-50230630	HMEC	breast:	n/a	chr3:50230513-50230526
6	RAD21	chr3:50229811-50230633	HCT-116	colon:	n/a	n/a
7	CTCF	chr3:50230540-50230690	WI-38	lung:	n/a	n/a
8	CTCF	chr3:50230520-50230670	GM12871	blood:	n/a	n/a
9	SMC3	chr3:50229666-50230758	SK-N-SH	brain:	n/a	n/a
10	CTCF	chr3:50229757-50230669	HCT-116	colon:	n/a	chr3:50230513-50230526
11	RAD21	chr3:50229905-50230585	ECC-1	luminal epithelium:	n/a	n/a
12	CTCF	chr3:50229605-50231147	SK-N-SH	brain:	n/a	chr3:50230513-50230526
13	RAD21	chr3:50229855-50231075	SK-N-SH	brain:	n/a	chr3:50230861-50230874

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:50230536-50230586	AG09319	gingival:	n/a
2	chr3:50230536-50230586	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:50230536-50230586	Hela-S3	cervix:	n/a
4	chr3:50230536-50230586	AG04449	skin:	fetal
5	chr3:50230536-50230586	PANC-1	pancreas:	n/a
6	chr3:50230536-50230586	IMR90	lung:	fetal
7	chr3:50230536-50230586	GM12878	blood:	n/a
8	chr3:50230536-50230586	LNCaP	prostate:	n/a
9	chr3:50230536-50230586	HIPEpiC	eye:	n/a
10	chr3:50230536-50230586	BJ	skin:	n/a
11	chr3:50230536-50230586	NT2-D1	testis:	n/a
12	chr3:50230536-50230586	T-47D	breast:	n/a
13	chr3:50230536-50230586	Caco-2	colon:	n/a
14	chr3:50230536-50230586	HAEpiC	amniotic membrane:	n/a
15	chr3:50230536-50230586	K562	blood:	n/a
16	chr3:50230536-50230586	HL-60	blood:	n/a
17	chr3:50230536-50230586	GM19239	blood:	n/a
18	chr3:50230536-50230586	AG09309	skin:	n/a
19	chr3:50230536-50230586	GM12891	blood:	n/a
20	chr3:50230536-50230586	GM12892	blood:	n/a
21	chr3:50230536-50230586	SK-N-MC	brain:	n/a
22	chr3:50230536-50230586	BE2_C	brain:	n/a
23	chr3:50230536-50230586	PrEC	prostate:	n/a
24	chr3:50230536-50230586	SK-N-SH_RA	brain:	n/a
25	chr3:50230536-50230586	RPTEC	kidney:	n/a
26	chr3:50230536-50230586	HEEpiC	esophagus:	n/a
27	chr3:50230536-50230586	AG04450	lung:	fetal
28	chr3:50230536-50230586	NB4	blood:	n/a
29	chr3:50230536-50230586	HCPEpiC	choroid plexus:	n/a
30	chr3:50230536-50230586	AG10803	skin:	n/a
31	chr3:50230536-50230586	HMEC	breast:	n/a
32	chr3:50230536-50230586	HCM	heart:	n/a
33	chr3:50230536-50230586	A549	lung:	n/a
34	chr3:50230536-50230586	ECC-1	luminal epithelium:	n/a
35	chr3:50230536-50230586	Hepatocyte	liver:	n/a
36	chr3:50230536-50230586	HepG2	liver:	n/a
37	chr3:50230536-50230586	HEK293	kidney:	embryo
38	chr3:50230536-50230586	HCT-116	colon:	n/a
39	chr3:50230536-50230586	U87	brain:	n/a
40	chr3:50230536-50230586	NHDF-neo	bronchial:	n/a
41	chr3:50230536-50230586	HCF	heart:	n/a
42	chr3:50230536-50230586	HRPEpiC	eye:	n/a
43	chr3:50230536-50230586	Jurkat	blood:	n/a
44	chr3:50230536-50230586	SKMC	muscle:	n/a
45	chr3:50230536-50230586	CMK	blood:	n/a
46	chr3:50230536-50230586	ovcar-3	ovarian:	n/a
47	chr3:50230536-50230586	HNPCEpiC	eye:	n/a
48	chr3:50230536-50230586	SK-N-SH	brain:	n/a
49	chr3:50230536-50230586	HUVEC	blood vessel:	n/a
50	chr3:50230536-50230586	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50229745..50230936-chr3:50263060..50264605,15	K562	blood:
2	chr3:50229808..50230758-chr3:50310116..50311009,3	MCF-7	breast:
3	chr3:50229933..50231783-chr3:50296964..50298649,2	K562	blood:
4	chr3:50230202..50232197-chr3:50263024..50265138,2	K562	blood:
5	chr3:50229830..50230764-chr3:50310279..50310998,2	MCF-7	breast:
6	chr3:50229708..50230647-chr3:50263213..50264126,9	MCF-7	breast:
7	chr3:50218401..50220545-chr3:50229488..50231128,2	MCF-7	breast:
8	chr3:50194714..50196531-chr3:50230211..50232377,2	K562	blood:
9	chr3:50229772..50232477-chr3:50306774..50308819,2	K562	blood:
10	chr3:50229825..50230750-chr3:50310077..50311002,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA3F-1	chr3:50230566-50230606	NONHSAT089794

No data

Variant related genes	Relation type
GNAT1	TF binding region
GNAT1	CpG island
ENSG00000114353	Chromatin interaction
ENSG00000230454	Chromatin interaction
ENSG00000012171	Chromatin interaction
ENSG00000001617	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11554989	1.00[AMR][1000 genomes]
rs13072164	1.00[AMR][1000 genomes]
rs35968178	1.00[AMR][1000 genomes]
rs6777625	1.00[AMR][1000 genomes]
rs6779184	1.00[AMR][1000 genomes]
rs6788251	1.00[AMR][1000 genomes]
rs6790729	1.00[AMR][1000 genomes]
rs6791799	1.00[AMR][1000 genomes]
rs6792611	1.00[AMR][1000 genomes]
rs6792754	1.00[AMR][1000 genomes]
rs6807067	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7610897	1.00[AMR][1000 genomes]
rs7645537	1.00[ASW][hapmap];0.82[YRI][hapmap]

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	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers 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	24 gene(s)	inside rSNPs	diseases
2	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Flanking Active TSS 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	24 gene(s)	inside rSNPs	diseases
3	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription 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	42 gene(s)	inside rSNPs	diseases
4	nsv876768	chr3:50144951-50267584	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong 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	17 gene(s)	inside rSNPs	diseases
5	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
6	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active 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	43 gene(s)	inside rSNPs	diseases
8	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
9	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
10	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
11	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
12	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
13	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription 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 miRNA target site	99 gene(s)	inside rSNPs	diseases
14	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
15	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription 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	53 gene(s)	inside rSNPs	diseases
16	nsv460529	chr3:50178011-50324672	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
17	nsv460530	chr3:50178011-50324672	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv590252	chr3:50178011-50324672	Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers 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	40 gene(s)	inside rSNPs	diseases
19	nsv1002916	chr3:50187646-50311666	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS 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	40 gene(s)	inside rSNPs	diseases
20	nsv536564	chr3:50187646-50311666	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
21	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
22	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers 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 miRNA target site	53 gene(s)	inside rSNPs	diseases
23	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
24	nsv590253	chr3:50196418-50337422	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
25	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
26	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription 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	74 gene(s)	inside rSNPs	diseases
27	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
28	nsv876771	chr3:50225568-50247824	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50210400-50242400	Weak transcription	Right Atrium	heart
2	chr3:50214200-50230600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:50220000-50231800	Weak transcription	K562	blood
4	chr3:50224400-50231600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:50225200-50230600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr3:50225800-50232200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:50226000-50230600	Weak transcription	Lung	lung
8	chr3:50226000-50231400	Weak transcription	Gastric	stomach
9	chr3:50226400-50232200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:50226600-50231200	Weak transcription	HMEC	breast
11	chr3:50226600-50239800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:50227400-50231600	Weak transcription	Brain Anterior Caudate	brain
13	chr3:50228200-50231800	Enhancers	Liver	Liver
14	chr3:50229400-50230600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:50229400-50230600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr3:50229400-50232800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr3:50230000-50230800	Enhancers	Esophagus	oesophagus
18	chr3:50230000-50231200	Enhancers	Spleen	Spleen
19	chr3:50230000-50231600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr3:50230000-50231600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
21	chr3:50230000-50231600	Bivalent Enhancer	Right Ventricle	heart
22	chr3:50230000-50232000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
23	chr3:50230000-50232400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
24	chr3:50230000-50233800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr3:50230200-50230600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr3:50230200-50230600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:50230200-50230600	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr3:50230200-50230600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
29	chr3:50230200-50230600	Enhancers	Brain Cingulate Gyrus	brain
30	chr3:50230200-50230600	Bivalent Enhancer	Colonic Mucosa	Colon
31	chr3:50230200-50230600	Enhancers	Fetal Heart	heart
32	chr3:50230200-50230600	Bivalent Enhancer	Fetal Intestine Small	intestine
33	chr3:50230200-50230600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
34	chr3:50230200-50231000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:50230200-50231200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
36	chr3:50230200-50231200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
37	chr3:50230200-50231400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:50230200-50231600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
39	chr3:50230200-50231600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
40	chr3:50230200-50231800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr3:50230200-50231800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
42	chr3:50230200-50231800	Weak transcription	HepG2	liver
43	chr3:50230200-50232200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:50230200-50232400	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr3:50230200-50232400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:50230200-50232400	Bivalent Enhancer	Placenta	Placenta
47	chr3:50230200-50232400	Bivalent Enhancer	Fetal Stomach	stomach
48	chr3:50230200-50233200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr3:50230200-50233800	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr3:50230400-50230600	Enhancers	Primary hematopoietic stem cells	blood

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