Variant report

Variant	rs7729529
Chromosome Location	chr5:43007818-43007819
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:0)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	REST	chr5:43007568-43009035	H1-neurons	neurons:	n/a	n/a
2	SIX5	chr5:43007791-43009153	A549	lung:	n/a	n/a
3	MXI1	chr5:43007595-43010060	Hela-S3	cervix:	n/a	n/a
4	E2F6	chr5:43007473-43008997	H1-hESC	embryonic stem cell:	n/a	chr5:43008350-43008359
5	MAX	chr5:43007529-43009038	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr5:43007544-43009843	GM12878	blood:	n/a	n/a
7	POLR2A	chr5:43007479-43009782	IMR90	lung:	n/a	n/a
8	E2F6	chr5:43007478-43009018	A549	lung:	n/a	chr5:43008350-43008359
9	ELK1	chr5:43007472-43009044	GM12878	blood:	n/a	n/a
10	NFIC	chr5:43007531-43009122	GM12878	blood:	n/a	n/a
11	POLR2A	chr5:43007338-43010590	PANC-1	pancreas:	n/a	n/a
12	TEAD4	chr5:43007476-43009093	K562	blood:	n/a	n/a
13	JUND	chr5:43007496-43009547	K562	blood:	n/a	chr5:43007667-43007675 chr5:43009342-43009349 chr5:43007667-43007675 chr5:43007667-43007674 chr5:43007665-43007676
14	JUN	chr5:43007603-43009080	K562	blood:	n/a	chr5:43007667-43007675 chr5:43007667-43007675 chr5:43007667-43007674
15	SMC3	chr5:43007505-43007864	K562	blood:	n/a	n/a
16	POLR2A	chr5:43007624-43008408	Gliobla	brain:	n/a	n/a
17	MAX	chr5:43007456-43010047	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr5:43007312-43009044	HL-60	blood:	n/a	n/a
19	POLR2A	chr5:43007474-43007967	GM12878	blood:	n/a	n/a
20	POLR2A	chr5:43007471-43009025	GM12891	blood:	n/a	n/a
21	MYC	chr5:43007520-43009400	K562	blood:	n/a	n/a
22	POLR2A	chr5:43007571-43007949	A549	lung:	n/a	n/a
23	RFX5	chr5:43007460-43010092	Hela-S3	cervix:	n/a	n/a
24	TAF1	chr5:43007593-43008544	ECC-1	luminal epithelium:	n/a	n/a
25	FOXA2	chr5:43007707-43008033	HepG2	liver:	n/a	n/a
26	SPI1	chr5:43007723-43008566	GM12878	blood:	n/a	n/a
27	KAP1	chr5:43007461-43007865	K562	blood:	n/a	n/a
28	POLR2A	chr5:43007368-43009204	SK-N-MC	brain:	n/a	n/a
29	MYC	chr5:43007402-43011171	NB4	blood:	n/a	n/a
30	POLR2A	chr5:43007525-43010794	NB4	blood:	n/a	n/a
31	POLR2A	chr5:43007569-43007929	A549	lung:	n/a	n/a
32	CEBPB	chr5:43007502-43007997	MCF-7	breast:	n/a	n/a
33	POLR2A	chr5:43007400-43010832	GM12878	blood:	n/a	n/a
34	SMARCC2	chr5:43007364-43008992	Hela-S3	cervix:	n/a	n/a
35	MAX	chr5:43007623-43008961	H1-hESC	embryonic stem cell:	n/a	n/a
36	TAF1	chr5:43007520-43008553	K562	blood:	n/a	n/a
37	REST	chr5:43007410-43009060	HL-60	blood:	n/a	n/a
38	SETDB1	chr5:43007727-43008305	U2OS	brain:	n/a	n/a
39	ATF2	chr5:43007386-43009807	GM12878	blood:	n/a	n/a
40	SMARCB1	chr5:43007281-43009916	Hela-S3	cervix:	n/a	n/a
41	TCF12	chr5:43007195-43009876	A549	lung:	n/a	n/a
42	MAX	chr5:43007557-43009024	SK-N-SH	brain:	n/a	n/a
43	POLR2A	chr5:43007388-43009806	GM12891	blood:	n/a	n/a
44	MAX	chr5:43007597-43009050	GM12878	blood:	n/a	n/a
45	CEBPB	chr5:43007613-43010152	IMR90	lung:	n/a	chr5:43008518-43008529
46	RELA	chr5:43007580-43010082	GM15510	blood:	n/a	n/a
47	TAF1	chr5:43007493-43008481	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr5:43007436-43009088	K562	blood:	n/a	n/a
49	POLR2A	chr5:43007337-43010908	GM18526	blood:	n/a	n/a
50	CBX3	chr5:43007338-43009017	K562	blood:	n/a	n/a

No data

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43007547..43009866-chr5:43041551..43043821,3	MCF-7	breast:
2	chr1:153962997..153963792-chr5:43007462..43008087,2	Hela-S3	cervix:
3	chr5:42908654..42910895-chr5:43006900..43010047,5	MCF-7	breast:
4	chr5:43006860..43010287-chr5:43063692..43067440,8	K562	blood:
5	chr5:43006330..43010322-chr5:43119527..43123237,8	MCF-7	breast:
6	chr5:43005892..43011349-chr5:43037590..43043804,20	K562	blood:
7	chr5:43006162..43011722-chr5:43063736..43068779,9	MCF-7	breast:
8	chr12:26111296..26112113-chr5:43007753..43008544,2	Hela-S3	cervix:
9	chr5:42912159..42915403-chr5:43007665..43011079,4	MCF-7	breast:
10	chr5:43006524..43009170-chr5:43481827..43484461,4	K562	blood:
11	chr5:43007638..43008310-chrX:47076739..47077691,2	Hela-S3	cervix:
12	chr5:43006765..43010626-chr5:43063692..43068627,9	K562	blood:
13	chr5:43005189..43014948-chr5:43062554..43069130,17	MCF-7	breast:
14	chr5:43007396..43009600-chr5:43120111..43123066,2	K562	blood:
15	chr5:43006939..43009143-chr5:43119919..43122235,2	K562	blood:
16	chr5:43007105..43008022-chrX:15692584..15693521,2	Hela-S3	cervix:
17	chr4:174255060..174255688-chr5:43007793..43008397,2	NB4	blood:
18	chr12:57481744..57482307-chr5:43007817..43008725,2	Hela-S3	cervix:
19	chr5:43005322..43013124-chr5:43037748..43043287,15	K562	blood:
20	chr5:43006142..43009170-chr5:43482864..43485007,3	K562	blood:
21	chr5:43007330..43009530-chr5:43039640..43043303,5	MCF-7	breast:
22	chr11:17297226..17298077-chr5:43007702..43008379,2	NB4	blood:
23	chr15:85524836..85525511-chr5:43007384..43008216,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000271788	TF binding region
ENSG00000251656	Chromatin interaction
ENSG00000215068	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000123094	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000186312	Chromatin interaction
ENSG00000246695	Chromatin interaction
ENSG00000102225	Chromatin interaction
ENSG00000166881	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000177954	Chromatin interaction
ENSG00000151881	Chromatin interaction
ENSG00000177721	Chromatin interaction
ENSG00000073417	Chromatin interaction
ENSG00000164104	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10058374	0.94[JPT][hapmap]
rs10074873	0.94[JPT][hapmap]
rs10075647	0.88[JPT][hapmap]
rs10078527	0.84[JPT][hapmap]
rs1032434	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10454865	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10805667	0.94[JPT][hapmap]
rs10941607	1.00[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10941608	1.00[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs11550285	0.95[ASN][1000 genomes]
rs11550286	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11550287	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11740797	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11742691	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11743246	0.83[ASN][1000 genomes]
rs11747015	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11748187	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11750239	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11949817	0.96[ASN][1000 genomes]
rs11954543	0.83[ASN][1000 genomes]
rs11956243	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12188691	0.85[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13155513	0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13159703	0.94[ASN][1000 genomes]
rs13165504	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13169563	0.94[ASN][1000 genomes]
rs13173064	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13665	0.94[JPT][hapmap]
rs1532331	0.94[JPT][hapmap]
rs17301375	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2452831	0.96[ASN][1000 genomes]
rs316398	0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs316405	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs316409	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs316410	0.96[ASN][1000 genomes]
rs316411	0.81[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs316418	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3207358	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34087147	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34315422	0.92[ASN][1000 genomes]
rs34492794	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34670023	0.91[ASN][1000 genomes]
rs34808919	0.96[ASN][1000 genomes]
rs34859360	0.92[ASN][1000 genomes]
rs35085573	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35541316	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35953019	0.94[JPT][hapmap]
rs36039989	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36083302	0.92[ASN][1000 genomes]
rs3733839	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3797312	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3849698	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs3849699	0.85[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4498259	0.94[JPT][hapmap]
rs493097	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs504404	0.85[ASN][1000 genomes]
rs541143	0.94[JPT][hapmap]
rs55939188	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56169202	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs581914	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62367685	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62367688	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62372869	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6414900	0.94[JPT][hapmap]
rs6451674	0.94[JPT][hapmap]
rs6451675	0.94[JPT][hapmap]
rs670206	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6859096	0.81[ASN][1000 genomes]
rs6862639	0.94[JPT][hapmap]
rs6864223	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6871636	0.94[JPT][hapmap]
rs6884303	0.94[JPT][hapmap]
rs6894506	0.94[JPT][hapmap]
rs7709181	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7727892	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7730004	0.94[JPT][hapmap]
rs9790935	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers 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 target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv534185	chr5:42804840-43067088	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	165 gene(s)	inside rSNPs	diseases
7	nsv1029288	chr5:42928085-43047323	Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	120 gene(s)	inside rSNPs	diseases
8	nsv968169	chr5:42956713-43043472	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	116 gene(s)	inside rSNPs	diseases
9	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
10	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
11	nsv881436	chr5:42967215-43008917	Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
12	nsv880447	chr5:42967215-43030798	Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
13	nsv881640	chr5:42978644-43028221	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
14	nsv880415	chr5:42978644-43030798	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7729529	ZNF131	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43007000-43009800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:43007200-43008200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr5:43007200-43008200	Active TSS	Right Atrium	heart
4	chr5:43007200-43008400	Active TSS	Rectal Mucosa Donor 31	rectum
5	chr5:43007200-43008400	Flanking Active TSS	Hela-S3	cervix
6	chr5:43007200-43008400	Flanking Active TSS	HUVEC	blood vessel
7	chr5:43007200-43008400	Flanking Active TSS	NH-A	brain
8	chr5:43007200-43008600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
9	chr5:43007200-43008600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:43007200-43008800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
11	chr5:43007200-43008800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:43007200-43008800	Flanking Active TSS	Adipose Nuclei	Adipose
13	chr5:43007200-43008800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
14	chr5:43007200-43008800	Flanking Active TSS	Fetal Thymus	thymus
15	chr5:43007200-43009200	Active TSS	H9 Cell Line	embryonic stem cell
16	chr5:43007200-43009400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
17	chr5:43007200-43009600	Active TSS	HSMMtube	muscle
18	chr5:43007200-43009800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:43007200-43010000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
20	chr5:43007200-43010000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
21	chr5:43007200-43010200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr5:43007200-43010200	Bivalent/Poised TSS	Left Ventricle	heart
23	chr5:43007200-43010400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
24	chr5:43007200-43010800	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr5:43007400-43008000	Flanking Active TSS	Primary T cells from cord blood	blood
26	chr5:43007400-43008000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr5:43007400-43008000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr5:43007400-43008000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
29	chr5:43007400-43008000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr5:43007400-43008200	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr5:43007400-43008400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
32	chr5:43007400-43008400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:43007400-43008600	Active TSS	HepG2	liver
34	chr5:43007400-43008800	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr5:43007400-43008800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:43007400-43008800	Flanking Active TSS	Primary B cells from peripheral blood	blood
37	chr5:43007400-43008800	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr5:43007400-43008800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:43007400-43008800	Flanking Bivalent TSS/Enh	Fetal Lung	lung
40	chr5:43007400-43008800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
41	chr5:43007400-43008800	Flanking Active TSS	NHEK	skin
42	chr5:43007400-43009000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr5:43007400-43009000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:43007400-43009000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:43007400-43009000	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr5:43007400-43009000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr5:43007400-43009000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
48	chr5:43007400-43009200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr5:43007400-43009200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:43007400-43009400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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