Variant report

Variant	rs11871637
Chromosome Location	chr17:59490235-59490236
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:0)
Chromatin interactive
region (count:121)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr17:59489358-59490419	H1-hESC	embryonic stem cell:	n/a	n/a
2	NFIC	chr17:59489653-59490526	HepG2	liver:	n/a	n/a
3	TCF12	chr17:59489128-59490537	A549	lung:	n/a	n/a
4	TBP	chr17:59489870-59490804	HepG2	liver:	n/a	n/a
5	MAZ	chr17:59489750-59490439	HepG2	liver:	n/a	n/a
6	ZBTB7A	chr17:59490072-59490368	HepG2	liver:	n/a	n/a
7	MEF2A	chr17:59485767-59490640	SK-N-SH	brain:	n/a	chr17:59489068-59489076
8	MAX	chr17:59489260-59491073	HepG2	liver:	n/a	n/a
9	GABPA	chr17:59489692-59490455	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr17:59489737-59490526	H1-hESC	embryonic stem cell:	n/a	n/a
11	ZNF143	chr17:59488142-59490296	H1-hESC	embryonic stem cell:	n/a	n/a
12	RAD21	chr17:59489382-59490427	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr17:59489746-59490497	H1-hESC	embryonic stem cell:	n/a	n/a
14	RAD21	chr17:59489446-59490386	A549	lung:	n/a	n/a
15	ZBTB7A	chr17:59489803-59490631	HepG2	liver:	n/a	n/a
16	ZBTB7A	chr17:59488540-59490591	ECC-1	luminal epithelium:	n/a	n/a
17	RAD21	chr17:59489579-59490265	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr17:59489768-59490903	HepG2	liver:	n/a	n/a
19	SIN3AK20	chr17:59489260-59490566	SK-N-SH	brain:	n/a	n/a
20	HDAC2	chr17:59489543-59490414	HepG2	liver:	n/a	n/a
21	RAD21	chr17:59487656-59491474	SK-N-SH	brain:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59491210-59491220 chr17:59488536-59488550 chr17:59488875-59488884 chr17:59488341-59488354 chr17:59487989-59487999 chr17:59488343-59488355
22	TCF12	chr17:59489565-59490252	ECC-1	luminal epithelium:	n/a	n/a
23	GABPA	chr17:59489726-59490331	H1-hESC	embryonic stem cell:	n/a	n/a
24	CCNT2	chr17:59489737-59490280	K562	blood:	n/a	n/a
25	MAX	chr17:59488627-59490510	SK-N-SH	brain:	n/a	chr17:59488910-59488926
26	RAD21	chr17:59489560-59490430	HepG2	liver:	n/a	n/a
27	REST	chr17:59489855-59490415	HepG2	liver:	n/a	n/a
28	TEAD4	chr17:59484276-59495088	A549	lung:	n/a	n/a
29	CTCF	chr17:59489286-59490518	HCT-116	colon:	n/a	n/a
30	CEBPD	chr17:59489728-59490506	HepG2	liver:	n/a	n/a
31	TEAD4	chr17:59487963-59490539	SK-N-SH	brain:	n/a	n/a
32	RAD21	chr17:59488655-59490470	HCT-116	colon:	n/a	chr17:59488875-59488884
33	EP300	chr17:59489767-59490314	HepG2	liver:	n/a	n/a
34	YY1	chr17:59489687-59490533	HepG2	liver:	n/a	n/a
35	TAF1	chr17:59489396-59490312	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr17:59489380-59490976	HepG2	liver:	n/a	n/a
37	BRCA1	chr17:59490202-59490271	H1-hESC	embryonic stem cell:	n/a	n/a
38	E2F6	chr17:59489101-59490572	A549	lung:	n/a	chr17:59489245-59489257
39	ZNF263	chr17:59488630-59490608	HEK293-T-REx	kidney:	n/a	chr17:59488691-59488700
40	HEY1	chr17:59489791-59490810	HepG2	liver:	n/a	n/a
41	ESRRA	chr17:59489475-59490307	GM12878	blood:	n/a	n/a
42	TCF12	chr17:59488534-59490349	ECC-1	luminal epithelium:	n/a	n/a
43	MAX	chr17:59488561-59490433	ECC-1	luminal epithelium:	n/a	chr17:59488910-59488926
44	E2F6	chr17:59489327-59490669	H1-hESC	embryonic stem cell:	n/a	n/a
45	GATA3	chr17:59489434-59490304	A549	lung:	n/a	n/a
46	CTCF	chr17:59487481-59491170	SK-N-SH	brain:	n/a	chr17:59488340-59488353 chr17:59488339-59488360 chr17:59488875-59488883 chr17:59488337-59488355 chr17:59488587-59488600 chr17:59488868-59488886 chr17:59488590-59488603 chr17:59488342-59488352 chr17:59488534-59488547
47	CTBP2	chr17:59488591-59490854	H1-hESC	embryonic stem cell:	n/a	n/a
48	RAD21	chr17:59483140-59491480	MCF-7	breast:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59491210-59491220 chr17:59488536-59488550 chr17:59488875-59488884 chr17:59488341-59488354 chr17:59487989-59487999 chr17:59488343-59488355
49	GATA3	chr17:59488556-59491169	MCF-7	breast:	n/a	chr17:59489068-59489078
50	POLR2A	chr17:59486113-59491295	IMR90	lung:	n/a	n/a

No data

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:59489469..59490241-chr20:55845005..55845901,3	MCF-7	breast:
2	chr17:59488009..59490784-chr17:78119613..78122104,2	MCF-7	breast:
3	chr17:59489661..59490440-chr17:59653693..59654566,2	MCF-7	breast:
4	chr17:59489694..59490861-chr17:59502803..59503675,3	MCF-7	breast:
5	chr17:59470525..59474011-chr17:59486288..59490375,89	MCF-7	breast:
6	chr17:59487822..59491370-chr20:49345755..49351152,8	MCF-7	breast:
7	chr12:116713817..116716728-chr17:59488795..59490962,2	MCF-7	breast:
8	chr17:59489649..59492493-chr3:119811877..119814556,2	MCF-7	breast:
9	chr17:59488630..59491909-chr20:52682988..52685576,3	MCF-7	breast:
10	chr17:59489126..59490399-chr17:59644784..59645856,3	MCF-7	breast:
11	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
12	chr17:59488147..59491206-chr17:73773645..73776030,4	MCF-7	breast:
13	chr17:59489674..59490313-chr17:59564952..59565665,2	MCF-7	breast:
14	chr17:59487742..59490467-chr20:52208536..52212416,5	MCF-7	breast:
15	chr17:59489834..59490453-chr17:59652319..59652838,2	MCF-7	breast:
16	chr17:59489585..59490693-chr20:49409810..49410733,3	MCF-7	breast:
17	chr17:57936511..57937414-chr17:59489781..59490328,2	MCF-7	breast:
18	chr17:59488387..59491331-chr17:73367342..73369969,2	MCF-7	breast:
19	chr1:202779094..202781986-chr17:59489238..59490887,2	MCF-7	breast:
20	chr17:59489293..59491949-chr8:125051873..125054864,2	MCF-7	breast:
21	chr17:59489613..59491206-chr17:59800419..59803266,2	MCF-7	breast:
22	chr17:59466830..59467981-chr17:59489440..59490777,4	MCF-7	breast:
23	chr17:59485603..59490421-chr20:49409438..49412592,198	MCF-7	breast:
24	chr14:68763338..68764227-chr17:59489430..59490294,2	MCF-7	breast:
25	chr17:59489419..59490363-chr20:52531972..52532900,2	MCF-7	breast:
26	chr17:59489592..59490427-chr21:38317002..38317522,3	MCF-7	breast:
27	chr17:59489569..59490613-chr17:59806350..59807273,3	MCF-7	breast:
28	chr17:59489912..59492013-chr20:52685644..52687540,2	MCF-7	breast:
29	chr17:59489678..59490370-chr20:45848502..45849271,2	MCF-7	breast:
30	chr17:57181543..57184200-chr17:59488935..59490643,2	MCF-7	breast:
31	chr17:57081949..57082809-chr17:59489487..59490386,4	MCF-7	breast:
32	chr17:59489184..59491261-chr17:59650345..59653673,119	MCF-7	breast:
33	chr17:59489445..59491262-chr17:59628200..59629244,34	MCF-7	breast:
34	chr17:59488984..59491525-chr17:73774194..73776083,3	MCF-7	breast:
35	chr17:59489384..59491650-chr6:42749691..42752599,2	MCF-7	breast:
36	chr17:59489460..59490356-chr17:59656181..59656834,2	MCF-7	breast:
37	chr17:59475999..59476687-chr17:59489352..59490506,3	MCF-7	breast:
38	chr17:59489874..59490819-chr17:59629776..59630756,2	MCF-7	breast:
39	chr17:59487584..59490320-chr17:60003961..60006356,2	MCF-7	breast:
40	chr17:59489819..59490342-chr17:59764278..59764797,2	MCF-7	breast:
41	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:
42	chr17:59489145..59490826-chr17:59913944..59915515,20	MCF-7	breast:
43	chr17:59489517..59490423-chr5:139348063..139348948,2	MCF-7	breast:
44	chr17:59489097..59491505-chr20:52824203..52825940,2	MCF-7	breast:
45	chr17:59489615..59490235-chr20:52815948..52816893,2	MCF-7	breast:
46	chr17:56707849..56710455-chr17:59488567..59490591,3	MCF-7	breast:
47	chr17:59489591..59490358-chr8:121600927..121601792,2	MCF-7	breast:
48	chr17:59486789..59493376-chr20:46130669..46135131,5	MCF-7	breast:
49	chr17:59489414..59490404-chr20:52556225..52557516,4	MCF-7	breast:
50	chr17:59489225..59491342-chr17:73769759..73771486,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267280	TF binding region
ENSG00000181171	Chromatin interaction
ENSG00000264853	Chromatin interaction
ENSG00000103326	Chromatin interaction
ENSG00000168137	Chromatin interaction
ENSG00000231128	Chromatin interaction
ENSG00000085433	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000123066	Chromatin interaction
ENSG00000141543	Chromatin interaction
ENSG00000112624	Chromatin interaction
ENSG00000265595	Chromatin interaction
ENSG00000171385	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000254249	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000254402	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000247828	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000244687	Chromatin interaction
ENSG00000081019	Chromatin interaction
ENSG00000260021	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000108479	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000072195	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000181163	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000082701	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000242622	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000228288	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000101132	Chromatin interaction
ENSG00000164180	Chromatin interaction
ENSG00000064787	Chromatin interaction
ENSG00000108506	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000104522	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000206573	Chromatin interaction
ENSG00000268603	Chromatin interaction
ENSG00000103266	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1000423	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1057987	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1058004	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10853031	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11079429	0.81[MEX][hapmap]
rs11868532	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12952625	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2078169	0.90[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.82[MEX][hapmap];0.94[TSI][hapmap]
rs2240736	1.00[CEU][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];0.97[TSI][hapmap];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2270114	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2286526	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs34446110	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7215775	0.99[EUR][1000 genomes]
rs729781	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8068318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.90[MEX][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8073698	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8074151	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8078036	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9891115	0.80[ASN][1000 genomes]
rs9905140	1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.94[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	nsv1065939	chr17:59283350-59517730	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	331 gene(s)	inside rSNPs	diseases
2	nsv833505	chr17:59323466-59518007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	326 gene(s)	inside rSNPs	diseases
3	nsv833506	chr17:59362377-59562984	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
4	nsv518130	chr17:59456589-59491281	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	265 gene(s)	inside rSNPs	diseases
5	esv1796927	chr17:59460119-59495319	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	270 gene(s)	inside rSNPs	diseases
6	nsv908663	chr17:59464069-59521310	Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	278 gene(s)	inside rSNPs	diseases
7	nsv908664	chr17:59465697-59491030	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	261 gene(s)	inside rSNPs	diseases
8	nsv908665	chr17:59470193-59494574	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	264 gene(s)	inside rSNPs	diseases
9	nsv908667	chr17:59471151-59491030	Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	256 gene(s)	inside rSNPs	diseases
10	nsv908668	chr17:59471151-59494574	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	263 gene(s)	inside rSNPs	diseases
11	nsv908669	chr17:59471372-59491030	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
12	nsv908670	chr17:59471372-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	262 gene(s)	inside rSNPs	diseases
13	nsv908671	chr17:59475888-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
14	nsv908672	chr17:59476062-59494574	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11871637	TMEM100	cis	cerebellum	SCAN
rs11871637	NACA2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59486400-59490600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr17:59486400-59490800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr17:59486600-59491000	Active TSS	Aorta	Aorta
4	chr17:59487400-59490400	Bivalent Enhancer	Fetal Brain Male	brain
5	chr17:59487600-59490800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
6	chr17:59487800-59490400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr17:59487800-59490600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr17:59487800-59490600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr17:59487800-59490800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr17:59488000-59490400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
11	chr17:59488000-59490600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
12	chr17:59488000-59490600	Active TSS	Fetal Lung	lung
13	chr17:59488000-59490800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr17:59488000-59490800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr17:59488200-59490400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
16	chr17:59488200-59490400	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr17:59488200-59490400	Active TSS	NHLF	lung
18	chr17:59488200-59490600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
19	chr17:59488200-59490600	Active TSS	Brain Angular Gyrus	brain
20	chr17:59488200-59490600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
21	chr17:59488200-59490600	Active TSS	Esophagus	oesophagus
22	chr17:59488200-59490600	Active TSS	Gastric	stomach
23	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
25	chr17:59488200-59490800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr17:59488200-59490800	Active TSS	Brain Anterior Caudate	brain
27	chr17:59488200-59491000	Active TSS	Fetal Kidney	kidney
28	chr17:59488400-59490400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
29	chr17:59488400-59490400	Flanking Active TSS	Liver	Liver
30	chr17:59488400-59491000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr17:59488400-59491000	Flanking Active TSS	Placenta	Placenta
32	chr17:59488600-59490600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr17:59488600-59490600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
34	chr17:59488600-59490600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
35	chr17:59488600-59490800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr17:59488600-59490800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
37	chr17:59488600-59491000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr17:59488800-59490400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr17:59488800-59490400	Active TSS	A549	lung
40	chr17:59488800-59490800	Active TSS	NHDF-Ad	bronchial
41	chr17:59488800-59491000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:59489000-59490400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr17:59489000-59490600	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr17:59489000-59490600	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
45	chr17:59489000-59490600	Active TSS	Osteobl	bone
46	chr17:59489000-59490800	Active TSS	Lung	lung
47	chr17:59489200-59490400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr17:59489200-59490400	Active TSS	Ovary	ovary
49	chr17:59489200-59490400	Active TSS	HSMMtube	muscle
50	chr17:59489200-59490600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain

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