Variant report

Variant	rs6836657
Chromosome Location	chr4:9693525-9693526
allele	G/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	POLR2A	chr4:9693153-9693576	MCF10A-Er-Src	breast:	n/a	n/a
2	STAT1	chr4:9693448-9693626	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:9693184-9693740	K562	blood:	n/a	n/a
4	POLR2A	chr4:9692444-9693955	H1-hESC	embryonic stem cell:	n/a	n/a
5	FOSL2	chr4:9692704-9693719	HepG2	liver:	n/a	chr4:9693096-9693105 chr4:9693486-9693495
6	SP4	chr4:9693282-9693714	H1-hESC	embryonic stem cell:	n/a	chr4:9693307-9693318 chr4:9693595-9693611
7	USF1	chr4:9693334-9693758	K562	blood:	n/a	chr4:9693561-9693572
8	USF1	chr4:9693436-9693652	HepG2	liver:	n/a	chr4:9693561-9693572
9	CCNT2	chr4:9693190-9693570	K562	blood:	n/a	n/a
10	E2F4	chr4:9693051-9693730	MCF10A-Er-Src	breast:	n/a	chr4:9693160-9693170 chr4:9693095-9693104 chr4:9693599-9693608
11	USF1	chr4:9693345-9693781	H1-hESC	embryonic stem cell:	n/a	chr4:9693561-9693572
12	BHLHE40	chr4:9693135-9693538	HepG2	liver:	n/a	chr4:9693155-9693171
13	POLR2A	chr4:9693016-9693548	PFSK-1	brain:	n/a	n/a
14	MAX	chr4:9693345-9693673	K562	blood:	n/a	n/a
15	JUND	chr4:9693213-9693729	K562	blood:	n/a	chr4:9693486-9693495
16	IRF1	chr4:9693168-9693657	K562	blood:	n/a	chr4:9693584-9693598 chr4:9693481-9693495 chr4:9693595-9693609 chr4:9693400-9693414
17	FOXP2	chr4:9693149-9693652	PFSK-1	brain:	n/a	n/a
18	SP1	chr4:9692106-9693756	HepG2	liver:	n/a	chr4:9693094-9693108 chr4:9693126-9693136 chr4:9693504-9693516 chr4:9693598-9693612 chr4:9693586-9693598 chr4:9693095-9693104 chr4:9693152-9693161 chr4:9693597-9693609 chr4:9693094-9693103 chr4:9693586-9693598 chr4:9693251-9693262 chr4:9693403-9693417 chr4:9693505-9693514 chr4:9693151-9693163 chr4:9693163-9693175 chr4:9693307-9693318 chr4:9693164-9693173 chr4:9693587-9693596 chr4:9693588-9693597 chr4:9693402-9693414 chr4:9693504-9693516 chr4:9693598-9693607 chr4:9693093-9693105 chr4:9693126-9693135 chr4:9693587-9693596 chr4:9693093-9693105 chr4:9693151-9693163 chr4:9693599-9693608 chr4:9693597-9693609
19	USF1	chr4:9693398-9693666	HepG2	liver:	n/a	chr4:9693561-9693572
20	SP1	chr4:9692953-9693618	H1-hESC	embryonic stem cell:	n/a	chr4:9693094-9693108 chr4:9693126-9693136 chr4:9693504-9693516 chr4:9693598-9693612 chr4:9693586-9693598 chr4:9693095-9693104 chr4:9693152-9693161 chr4:9693597-9693609 chr4:9693094-9693103 chr4:9693586-9693598 chr4:9693251-9693262 chr4:9693403-9693417 chr4:9693505-9693514 chr4:9693151-9693163 chr4:9693163-9693175 chr4:9693307-9693318 chr4:9693164-9693173 chr4:9693587-9693596 chr4:9693588-9693597 chr4:9693402-9693414 chr4:9693504-9693516 chr4:9693598-9693607 chr4:9693093-9693105 chr4:9693126-9693135 chr4:9693587-9693596 chr4:9693093-9693105 chr4:9693151-9693163 chr4:9693599-9693608 chr4:9693597-9693609
21	TCF3	chr4:9693172-9693571	GM12878	blood:	n/a	n/a
22	USF1	chr4:9693396-9693636	GM12878	blood:	n/a	chr4:9693561-9693572
23	SIN3AK20	chr4:9693139-9693630	HepG2	liver:	n/a	n/a
24	ZBTB7A	chr4:9693306-9693581	K562	blood:	n/a	n/a
25	MYC	chr4:9693372-9693664	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr4:9692428-9693681	K562	blood:	n/a	n/a
27	MXI1	chr4:9693300-9693602	HepG2	liver:	n/a	n/a
28	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
29	HEY1	chr4:9692165-9693617	HepG2	liver:	n/a	chr4:9693587-9693602
30	HMGN3	chr4:9692985-9693642	K562	blood:	n/a	n/a
31	USF1	chr4:9693364-9693674	SK-N-SH_RA	brain:	n/a	chr4:9693561-9693572
32	MAZ	chr4:9693244-9693659	HepG2	liver:	n/a	n/a
33	MYC	chr4:9693458-9693647	K562	blood:	n/a	n/a
34	USF2	chr4:9693434-9693645	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAZ	chr4:9693038-9693659	K562	blood:	n/a	n/a
36	USF1	chr4:9693400-9693657	SK-N-SH_RA	brain:	n/a	chr4:9693561-9693572
37	SP1	chr4:9692853-9693834	GM12878	blood:	n/a	chr4:9693094-9693108 chr4:9693126-9693136 chr4:9693504-9693516 chr4:9693598-9693612 chr4:9693586-9693598 chr4:9693095-9693104 chr4:9693152-9693161 chr4:9693597-9693609 chr4:9693094-9693103 chr4:9693586-9693598 chr4:9693251-9693262 chr4:9693403-9693417 chr4:9693505-9693514 chr4:9693151-9693163 chr4:9693163-9693175 chr4:9693307-9693318 chr4:9693164-9693173 chr4:9693587-9693596 chr4:9693588-9693597 chr4:9693402-9693414 chr4:9693504-9693516 chr4:9693598-9693607 chr4:9693093-9693105 chr4:9693126-9693135 chr4:9693587-9693596 chr4:9693093-9693105 chr4:9693151-9693163 chr4:9693599-9693608 chr4:9693597-9693609
38	BHLHE40	chr4:9693347-9693648	GM12878	blood:	n/a	n/a
39	USF1	chr4:9693359-9693751	H1-hESC	embryonic stem cell:	n/a	chr4:9693561-9693572
40	MAX	chr4:9693429-9693662	NB4	blood:	n/a	n/a
41	UBTF	chr4:9693479-9693639	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9693516-9693566	A549	lung:	n/a
2	chr4:9693516-9693566	SAEC	small airway:	n/a
3	chr4:9693516-9693566	AG04450	lung:	fetal
4	chr4:9693516-9693566	PFSK-1	brain:	n/a
5	chr4:9693516-9693566	BE2_C	brain:	n/a
6	chr4:9693516-9693566	T-47D	breast:	n/a
7	chr4:9693516-9693566	NH-A	brain:	n/a
8	chr4:9693516-9693566	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:9693516-9693566	NT2-D1	testis:	n/a
10	chr4:9693516-9693566	ovcar-3	ovarian:	n/a
11	chr4:9693516-9693566	HMEC	breast:	n/a
12	chr4:9693516-9693566	AG04449	skin:	fetal
13	chr4:9693516-9693566	HUVEC	blood vessel:	n/a
14	chr4:9693516-9693566	H1-hESC	embryonic stem cell:	embryo
15	chr4:9693516-9693566	HCT-116	colon:	n/a
16	chr4:9693516-9693566	GM12878	blood:	n/a
17	chr4:9693516-9693566	ProgFib	skin:	n/a
18	chr4:9693516-9693566	CMK	blood:	n/a
19	chr4:9693516-9693566	HAEpiC	amniotic membrane:	n/a
20	chr4:9693516-9693566	GM12892	blood:	n/a
21	chr4:9693516-9693566	RPTEC	kidney:	n/a
22	chr4:9693516-9693566	HRE	kidney:	n/a
23	chr4:9693516-9693566	IMR90	lung:	fetal
24	chr4:9693516-9693566	HL-60	blood:	n/a
25	chr4:9693516-9693566	SK-N-SH_RA	brain:	n/a
26	chr4:9693516-9693566	HEEpiC	esophagus:	n/a
27	chr4:9693516-9693566	NHDF-neo	bronchial:	n/a
28	chr4:9693516-9693566	BJ	skin:	n/a
29	chr4:9693516-9693566	SKMC	muscle:	n/a
30	chr4:9693516-9693566	HEK293	kidney:	embryo
31	chr4:9693516-9693566	Hela-S3	cervix:	n/a
32	chr4:9693516-9693566	PANC-1	pancreas:	n/a
33	chr4:9693516-9693566	Jurkat	blood:	n/a
34	chr4:9693516-9693566	GM12891	blood:	n/a
35	chr4:9693516-9693566	Hepatocyte	liver:	n/a
36	chr4:9693516-9693566	NHBE	bronchial:	n/a
37	chr4:9693516-9693566	GM06990	blood:	n/a
38	chr4:9693516-9693566	PrEC	prostate:	n/a
39	chr4:9693516-9693566	HNPCEpiC	eye:	n/a
40	chr4:9693516-9693566	HRPEpiC	eye:	n/a
41	chr4:9693516-9693566	HCPEpiC	choroid plexus:	n/a
42	chr4:9693516-9693566	NB4	blood:	n/a
43	chr4:9693516-9693566	U87	brain:	n/a
44	chr4:9693516-9693566	SK-N-MC	brain:	n/a
45	chr4:9693516-9693566	ECC-1	luminal epithelium:	n/a
46	chr4:9693516-9693566	Caco-2	colon:	n/a
47	chr4:9693516-9693566	MCF10A-Er-Src	breast:	n/a
48	chr4:9693516-9693566	HCF	heart:	n/a
49	chr4:9693516-9693566	HRCEpiC	kidney:	n/a
50	chr4:9693516-9693566	AG10803	skin:	n/a

Variant related genes	Relation type
FAM86MP	TF binding region
FAM86MP	CpG island

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs4235360	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4277776	1.00[EUR][1000 genomes]
rs4377591	0.87[EUR][1000 genomes]
rs6855159	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1796218	chr4:9324644-9714338	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
2	nsv428108	chr4:9324644-9764173	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
3	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
4	nsv818213	chr4:9371116-9719981	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
5	esv2754610	chr4:9372303-9804524	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
6	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
7	nsv1012865	chr4:9429299-9794181	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv1001143	chr4:9435322-9794181	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
9	nsv1011425	chr4:9436994-9715105	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1002981	chr4:9446035-9698645	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
11	nsv1007204	chr4:9456977-9707068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
12	nsv1006867	chr4:9456977-9713612	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
13	nsv1002757	chr4:9456977-9715105	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
14	nsv1012621	chr4:9456977-9802366	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
15	nsv1012965	chr4:9461218-9696765	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
16	nsv1012634	chr4:9461218-9802366	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
17	nsv998043	chr4:9496282-9830208	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
18	esv10795	chr4:9508396-9745703	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
19	nsv878667	chr4:9543673-9903121	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
20	nsv878669	chr4:9551094-9794724	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
21	nsv469511	chr4:9609987-9754029	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
22	nsv482424	chr4:9609987-9754029	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
23	nsv964031	chr4:9629449-9764955	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv1000853	chr4:9632436-9696765	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
25	nsv999102	chr4:9633247-9794181	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9692000-9693800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr4:9692400-9693800	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr4:9692400-9693800	Active TSS	Brain Anterior Caudate	brain
4	chr4:9692400-9693800	Active TSS	Fetal Brain Female	brain
5	chr4:9692400-9693800	Active TSS	Fetal Kidney	kidney
6	chr4:9692400-9693800	Active TSS	Rectal Smooth Muscle	rectum
7	chr4:9692600-9693600	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr4:9692600-9693600	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr4:9692600-9693600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:9692600-9693600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:9692600-9693600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:9692600-9693600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:9692600-9693600	Active TSS	Brain Substantia Nigra	brain
14	chr4:9692600-9693600	Active TSS	Pancreas	Pancrea
15	chr4:9692600-9693600	Active TSS	Right Ventricle	heart
16	chr4:9692600-9693600	Active TSS	HepG2	liver
17	chr4:9692600-9693600	Active TSS	HSMM	muscle
18	chr4:9692600-9693800	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr4:9692600-9693800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:9692600-9693800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:9692600-9693800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:9692600-9693800	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr4:9692600-9693800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:9692600-9693800	Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr4:9692600-9693800	Active TSS	Primary T cells from cord blood	blood
26	chr4:9692600-9693800	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr4:9692600-9693800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:9692600-9693800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:9692600-9693800	Active TSS	Brain Angular Gyrus	brain
30	chr4:9692600-9693800	Active TSS	Brain Hippocampus Middle	brain
31	chr4:9692600-9693800	Active TSS	Colon Smooth Muscle	Colon
32	chr4:9692600-9693800	Active TSS	Fetal Lung	lung
33	chr4:9692600-9693800	Active TSS	Left Ventricle	heart
34	chr4:9692600-9693800	Active TSS	Right Atrium	heart
35	chr4:9692600-9693800	Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr4:9692600-9693800	Active TSS	HSMMtube	muscle
37	chr4:9692600-9693800	Active TSS	NH-A	brain
38	chr4:9692600-9694000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr4:9692600-9694000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:9692600-9694000	Active TSS	Brain Cingulate Gyrus	brain
41	chr4:9692600-9694000	Active TSS	Brain Germinal Matrix	brain
42	chr4:9692600-9694000	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr4:9692600-9694200	Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr4:9692800-9693600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr4:9692800-9693600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:9692800-9693600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr4:9692800-9693600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr4:9692800-9693600	Active TSS	Duodenum Mucosa	Duodenum
49	chr4:9692800-9693600	Active TSS	Psoas Muscle	Psoas
50	chr4:9692800-9693600	Active TSS	Small Intestine	intestine

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