Variant report

Variant	rs16892232
Chromosome Location	chr4:15657636-15657637
allele	C/G
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	YY1	chr4:15656700-15657648	A549	lung:	n/a	chr4:15656727-15656738 chr4:15656730-15656744 chr4:15657321-15657333 chr4:15656729-15656743 chr4:15657480-15657491
2	POLR2A	chr4:15656283-15658011	Raji	blood:	n/a	n/a
3	TAF7	chr4:15656224-15657979	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr4:15656638-15657891	SK-N-SH	brain:	n/a	n/a
5	YY1	chr4:15656677-15657682	SK-N-SH	brain:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15656730-15656744 chr4:15657321-15657333 chr4:15656729-15656743 chr4:15657480-15657491
6	JUND	chr4:15656842-15658077	H1-hESC	embryonic stem cell:	n/a	chr4:15657445-15657459
7	POLR2A	chr4:15656210-15657834	MCF10A-Er-Src	breast:	n/a	n/a
8	MAZ	chr4:15655158-15657667	K562	blood:	n/a	chr4:15657135-15657145 chr4:15657091-15657100 chr4:15657092-15657103 chr4:15657093-15657102 chr4:15657091-15657106
9	REST	chr4:15655634-15657879	H1-neurons	neurons:	n/a	chr4:15657259-15657277 chr4:15656362-15656375 chr4:15656791-15656804
10	E2F6	chr4:15656367-15657938	K562	blood:	n/a	chr4:15657782-15657789 chr4:15657565-15657575 chr4:15656733-15656742 chr4:15657800-15657817 chr4:15657131-15657143 chr4:15657581-15657590 chr4:15656988-15656997 chr4:15657130-15657141 chr4:15657587-15657597 chr4:15656984-15656993 chr4:15657782-15657789 chr4:15657782-15657789
11	CCNT2	chr4:15656329-15658018	K562	blood:	n/a	chr4:15657746-15657755 chr4:15657603-15657612
12	POLR2A	chr4:15656197-15658025	GM18505	blood:	n/a	n/a
13	POLR2A	chr4:15656200-15657889	HUVEC	blood vessel:	n/a	n/a
14	POLR2A	chr4:15656486-15657671	HCT-116	colon:	n/a	n/a
15	POLR2A	chr4:15656252-15657826	GM15510	blood:	n/a	n/a
16	TAF1	chr4:15656238-15658112	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr4:15656658-15658363	U87	brain:	n/a	n/a
18	POLR2A	chr4:15655492-15658152	HUVEC	blood vessel:	n/a	n/a
19	TAF1	chr4:15656237-15657792	ECC-1	luminal epithelium:	n/a	n/a
20	POLR2A	chr4:15656251-15657675	GM12878	blood:	n/a	n/a
21	POLR2A	chr4:15656626-15657768	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr4:15656179-15658274	MCF-7	breast:	n/a	n/a
23	POLR2A	chr4:15656716-15657875	U87	brain:	n/a	n/a
24	POLR2A	chr4:15656300-15658093	GM19099	blood:	n/a	n/a
25	ATF2	chr4:15657001-15658061	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr4:15657018-15657822	H1-hESC	embryonic stem cell:	n/a	n/a
27	GATA1	chr4:15654932-15657728	PBDE	blood:	n/a	chr4:15656777-15656786 chr4:15655275-15655285
28	POLR2A	chr4:15656576-15657694	GM12891	blood:	n/a	n/a
29	CREB1	chr4:15656261-15657656	HepG2	liver:	n/a	n/a
30	YY1	chr4:15656575-15658002	H1-hESC	embryonic stem cell:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15657806-15657816 chr4:15656730-15656744 chr4:15657746-15657757 chr4:15657321-15657333 chr4:15657806-15657816 chr4:15656621-15656630 chr4:15656729-15656743 chr4:15657480-15657491
31	POLR2A	chr4:15656185-15658111	K562	blood:	n/a	n/a
32	POLR2A	chr4:15657575-15657644	HepG2	liver:	n/a	n/a
33	POLR2A	chr4:15657033-15657808	GM12891	blood:	n/a	n/a
34	YY1	chr4:15656440-15658028	ECC-1	luminal epithelium:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15657806-15657816 chr4:15656730-15656744 chr4:15657746-15657757 chr4:15657321-15657333 chr4:15657806-15657816 chr4:15656621-15656630 chr4:15656729-15656743 chr4:15657480-15657491
35	YY1	chr4:15656535-15657711	K562	blood:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15656730-15656744 chr4:15657321-15657333 chr4:15656621-15656630 chr4:15656729-15656743 chr4:15657480-15657491
36	POLR2A	chr4:15656154-15657734	K562	blood:	n/a	n/a
37	POLR2A	chr4:15656166-15657924	K562	blood:	n/a	n/a
38	MAX	chr4:15656569-15657986	H1-hESC	embryonic stem cell:	n/a	chr4:15657135-15657145 chr4:15657091-15657100 chr4:15657092-15657103 chr4:15657093-15657102 chr4:15657091-15657106
39	MAX	chr4:15656835-15657639	A549	lung:	n/a	chr4:15657135-15657145 chr4:15657091-15657100 chr4:15657092-15657103 chr4:15657093-15657102 chr4:15657091-15657106
40	POLR2A	chr4:15656258-15657691	A549	lung:	n/a	n/a
41	POLR2A	chr4:15656196-15657727	ProgFib	skin:	n/a	n/a
42	E2F6	chr4:15656471-15658005	H1-hESC	embryonic stem cell:	n/a	chr4:15657782-15657789 chr4:15657565-15657575 chr4:15656733-15656742 chr4:15657800-15657817 chr4:15657131-15657143 chr4:15657581-15657590 chr4:15656988-15656997 chr4:15657130-15657141 chr4:15657587-15657597 chr4:15656984-15656993 chr4:15657782-15657789 chr4:15657782-15657789
43	YY1	chr4:15656239-15657931	GM12878	blood:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15657806-15657816 chr4:15656730-15656744 chr4:15657746-15657757 chr4:15657321-15657333 chr4:15657806-15657816 chr4:15656621-15656630 chr4:15656729-15656743 chr4:15657480-15657491
44	POLR2A	chr4:15656286-15658008	NB4	blood:	n/a	n/a
45	POLR2A	chr4:15656122-15658044	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:15656741-15657954	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr4:15656223-15657862	GM12892	blood:	n/a	n/a
48	BACH1	chr4:15657161-15657824	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr4:15656276-15658230	GM12878	blood:	n/a	n/a
50	YY1	chr4:15656509-15658082	ECC-1	luminal epithelium:	n/a	chr4:15656680-15656694 chr4:15656727-15656738 chr4:15657806-15657816 chr4:15656730-15656744 chr4:15657746-15657757 chr4:15657321-15657333 chr4:15657806-15657816 chr4:15656621-15656630 chr4:15656729-15656743 chr4:15657480-15657491

No.	Distal block	Cell Line	Cell type
1	chr4:15651703..15660794-chr4:15677607..15686235,25	K562	blood:
2	chr4:15654775..15659231-chr4:15659761..15666940,9	K562	blood:
3	chr4:15649873..15653235-chr4:15657425..15660766,3	MCF-7	breast:
4	chr15:72766669..72767169-chr4:15657562..15658305,2	HCT-116	colon:
5	chr4:15002808..15006132-chr4:15656406..15658114,3	K562	blood:
6	chr4:15655671..15658131-chr4:15716646..15719360,2	MCF-7	breast:
7	chr4:15479740..15482605-chr4:15655501..15658427,3	MCF-7	breast:
8	chr4:15469326..15470996-chr4:15657243..15660173,2	MCF-7	breast:
9	chr4:15656159..15658615-chr4:15712805..15714316,2	K562	blood:
10	chr4:15650206..15660298-chr4:15677140..15687517,25	K562	blood:
11	chr4:15654963..15657954-chr4:15685988..15688544,3	MCF-7	breast:
12	chr21:34601586..34602556-chr4:15656823..15657778,2	NB4	blood:
13	chr12:122235040..122237798-chr4:15655451..15658367,2	MCF-7	breast:
14	chr4:15655595..15658742-chr4:15680185..15687360,10	MCF-7	breast:
15	chr4:15652080..15658606-chr4:15677363..15685579,17	MCF-7	breast:

Variant related genes	Relation type
FBXL5	TF binding region
ENSG00000159110	Chromatin interaction
ENSG00000272849	Chromatin interaction
ENSG00000137449	Chromatin interaction
ENSG00000166233	Chromatin interaction
ENSG00000237765	Chromatin interaction
ENSG00000247624	Chromatin interaction
ENSG00000048342	Chromatin interaction
ENSG00000109743	Chromatin interaction
ENSG00000118564	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs17385861	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17385951	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17405797	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17476879	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2302465	0.90[EUR][1000 genomes]
rs2302469	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3756245	0.81[EUR][1000 genomes]
rs3822258	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4279202	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55735476	0.90[EUR][1000 genomes]
rs55757331	0.81[EUR][1000 genomes]
rs55784324	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55803452	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55963737	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56065468	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56093715	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56094420	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56149419	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56166932	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73224650	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73224656	0.85[EUR][1000 genomes]
rs73237171	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73237172	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73237182	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73237198	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239165	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239167	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239174	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239175	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239182	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239189	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239191	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73239193	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241109	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241111	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241112	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241117	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241120	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241180	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241183	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241185	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241190	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241191	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241195	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241197	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73241198	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243105	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243107	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243112	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243114	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243118	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243126	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243128	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243129	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243131	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243132	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73243135	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7683000	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2757923	chr4:15444617-15749520	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv2759227	chr4:15444617-15749520	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv428439	chr4:15556961-15749520	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv518830	chr4:15610771-15672200	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv521183	chr4:15610771-15692136	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	esv3322833	chr4:15655679-15658227	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
9	esv3351978	chr4:15655904-15658002	Flanking Active TSS Active TSS Enhancers 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	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15654600-15658000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr4:15654600-15658200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr4:15654800-15658000	Active TSS	Psoas Muscle	Psoas
4	chr4:15655000-15657800	Active TSS	Left Ventricle	heart
5	chr4:15655000-15657800	Active TSS	Right Ventricle	heart
6	chr4:15655000-15658000	Active TSS	Ovary	ovary
7	chr4:15655200-15657800	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr4:15655600-15657800	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr4:15655600-15657800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:15655600-15657800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:15655600-15657800	Active TSS	Brain Substantia Nigra	brain
12	chr4:15655600-15657800	Active TSS	Gastric	stomach
13	chr4:15655600-15657800	Active TSS	HSMMtube	muscle
14	chr4:15655600-15658200	Active TSS	H9 Cell Line	embryonic stem cell
15	chr4:15655600-15658200	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr4:15655800-15657800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:15655800-15657800	Active TSS	Colon Smooth Muscle	Colon
18	chr4:15655800-15657800	Active TSS	Fetal Lung	lung
19	chr4:15655800-15658000	Active TSS	Esophagus	oesophagus
20	chr4:15655800-15658200	Active TSS	Duodenum Mucosa	Duodenum
21	chr4:15655800-15658400	Active TSS	Brain Anterior Caudate	brain
22	chr4:15656000-15657800	Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr4:15656000-15657800	Active TSS	Fetal Brain Female	brain
24	chr4:15656000-15657800	Active TSS	Fetal Kidney	kidney
25	chr4:15656000-15658000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr4:15656000-15658200	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr4:15656000-15658200	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr4:15656000-15658200	Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr4:15656200-15657800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr4:15656200-15658000	Active TSS	Sigmoid Colon	Sigmoid Colon
31	chr4:15656200-15658200	Active TSS	Stomach Smooth Muscle	stomach
32	chr4:15656400-15657800	Active TSS	Primary T cells from cord blood	blood
33	chr4:15656400-15658000	Active TSS	Liver	Liver
34	chr4:15657000-15657800	Flanking Active TSS	HMEC	breast
35	chr4:15657200-15657800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:15657200-15657800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:15657200-15657800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr4:15657200-15657800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr4:15657200-15657800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:15657200-15657800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:15657200-15657800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:15657200-15657800	Flanking Active TSS	Colonic Mucosa	Colon
43	chr4:15657200-15657800	Flanking Active TSS	Placenta	Placenta
44	chr4:15657200-15657800	Flanking Active TSS	Placenta Amnion	Placenta Amnion
45	chr4:15657200-15657800	Flanking Active TSS	HUVEC	blood vessel
46	chr4:15657200-15657800	Flanking Active TSS	NH-A	brain
47	chr4:15657200-15657800	Flanking Active TSS	NHDF-Ad	bronchial
48	chr4:15657200-15658000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr4:15657200-15658000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:15657200-15658000	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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