Variant report

Variant	rs2239470
Chromosome Location	chrX:153598413-153598414
allele	C/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	chrX:153596917-153600131	HUVEC	blood vessel:	n/a	n/a
2	POLR2A	chrX:153596313-153598593	HepG2	liver:	n/a	n/a
3	POLR2A	chrX:153596815-153600135	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chrX:153592099-153599779	H1-hESC	embryonic stem cell:	n/a	n/a
5	FOS	chrX:153597935-153598465	MCF10A-Er-Src	breast:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598103-153598111 chrX:153598101-153598112
6	SMARCB1	chrX:153597102-153600176	Hela-S3	cervix:	n/a	chrX:153597165-153597174 chrX:153598102-153598111
7	POLR2A	chrX:153598033-153598592	Raji	blood:	n/a	n/a
8	TBP	chrX:153597944-153598423	Hela-S3	cervix:	n/a	n/a
9	SRF	chrX:153597053-153598849	HCT-116	colon:	n/a	chrX:153597765-153597779 chrX:153597950-153597963 chrX:153597950-153597961 chrX:153597947-153597961 chrX:153597948-153597966 chrX:153597952-153597963 chrX:153597945-153597962 chrX:153597952-153597961 chrX:153597951-153597965 chrX:153597764-153597782 chrX:153597951-153597962 chrX:153597950-153597963 chrX:153597948-153597962 chrX:153598147-153598157 chrX:153597948-153597966 chrX:153597950-153597965 chrX:153597947-153597965 chrX:153597949-153597964 chrX:153597952-153597966 chrX:153597768-153597782
10	EP300	chrX:153596971-153598455	SK-N-SH	brain:	n/a	chrX:153598103-153598112
11	JUND	chrX:153597049-153598812	SK-N-SH	brain:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598101-153598112 chrX:153598103-153598111 chrX:153597165-153597173 chrX:153597453-153597461 chrX:153597166-153597177 chrX:153597163-153597175
12	POLR2A	chrX:153597911-153599015	GM12878	blood:	n/a	n/a
13	EGR1	chrX:153596988-153598516	HCT-116	colon:	n/a	chrX:153597058-153597067 chrX:153598135-153598149 chrX:153597042-153597052
14	MAX	chrX:153597871-153598433	A549	lung:	n/a	chrX:153598103-153598112
15	TAF1	chrX:153597920-153598503	H1-hESC	embryonic stem cell:	n/a	n/a
16	SIN3AK20	chrX:153596937-153598795	MCF-7	breast:	n/a	n/a
17	POLR2A	chrX:153596901-153598868	PANC-1	pancreas:	n/a	n/a
18	SIN3A	chrX:153597220-153599016	H1-hESC	embryonic stem cell:	n/a	chrX:153597529-153597538 chrX:153597496-153597506
19	POLR2A	chrX:153596878-153598673	MCF10A-Er-Src	breast:	n/a	n/a
20	GATA3	chrX:153597028-153598591	A549	lung:	n/a	chrX:153598393-153598406 chrX:153598395-153598403 chrX:153597322-153597331
21	POLR2A	chrX:153597060-153600136	GM18505	blood:	n/a	n/a
22	POLR2A	chrX:153597023-153600069	HUVEC	blood vessel:	n/a	n/a
23	JUND	chrX:153597910-153599238	H1-hESC	embryonic stem cell:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598101-153598112 chrX:153598103-153598111
24	TAF1	chrX:153597950-153598420	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chrX:153596500-153600134	HepG2	liver:	n/a	n/a
26	TAF1	chrX:153597652-153598536	K562	blood:	n/a	n/a
27	POLR2A	chrX:153597112-153598614	GM19099	blood:	n/a	n/a
28	MXI1	chrX:153596526-153600635	IMR90	lung:	n/a	chrX:153597324-153597339
29	JUND	chrX:153597876-153598573	GM12878	blood:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598101-153598112 chrX:153598103-153598111
30	HEY1	chrX:153597870-153598435	HepG2	liver:	n/a	n/a
31	MAFK	chrX:153597902-153598633	H1-hESC	embryonic stem cell:	n/a	chrX:153598103-153598113
32	CHD2	chrX:153597468-153598907	H1-hESC	embryonic stem cell:	n/a	n/a
33	FOSL2	chrX:153596924-153598426	SK-N-SH	brain:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598103-153598111 chrX:153597165-153597173 chrX:153597394-153597405 chrX:153597453-153597461 chrX:153597166-153597177 chrX:153598100-153598111 chrX:153597163-153597175
34	CHD1	chrX:153598029-153599678	H1-hESC	embryonic stem cell:	n/a	chrX:153599080-153599087
35	POLR2A	chrX:153598373-153598535	A549	lung:	n/a	n/a
36	POLR2A	chrX:153592005-153599772	GM12878	blood:	n/a	n/a
37	POLR2A	chrX:153598305-153598581	A549	lung:	n/a	n/a
38	SP1	chrX:153597061-153598612	A549	lung:	n/a	chrX:153597467-153597479 chrX:153597116-153597125 chrX:153597861-153597873 chrX:153597861-153597873 chrX:153597862-153597871 chrX:153597862-153597871 chrX:153598138-153598149 chrX:153597469-153597478 chrX:153597468-153597477 chrX:153597862-153597872 chrX:153597117-153597126 chrX:153597115-153597127 chrX:153597793-153597807 chrX:153597467-153597479 chrX:153597863-153597872 chrX:153598013-153598027 chrX:153597115-153597127
39	POLR2A	chrX:153596487-153598573	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chrX:153597890-153598596	A549	lung:	n/a	n/a
41	NFIC	chrX:153597037-153598485	SK-N-SH	brain:	n/a	n/a
42	TAF7	chrX:153598332-153598745	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chrX:153597267-153599033	H1-hESC	embryonic stem cell:	n/a	n/a
44	USF2	chrX:153598099-153598733	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chrX:153597077-153598800	MCF10A-Er-Src	breast:	n/a	n/a
46	HCFC1	chrX:153596894-153598898	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chrX:153592032-153601467	GM12892	blood:	n/a	n/a
48	FOSL2	chrX:153597753-153598708	A549	lung:	n/a	chrX:153598102-153598112 chrX:153598103-153598111 chrX:153598103-153598110 chrX:153598057-153598066 chrX:153598103-153598111 chrX:153598100-153598111
49	MAZ	chrX:153596317-153600539	IMR90	lung:	n/a	chrX:153597541-153597552 chrX:153597330-153597339 chrX:153599763-153599773 chrX:153597629-153597639 chrX:153598103-153598112 chrX:153600366-153600376
50	POLR2A	chrX:153591801-153598985	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:153597889..153602863-chrX:153674100..153678441,6	MCF-7	breast:
2	chrX:153596811..153598878-chrX:153705580..153707217,2	MCF-7	breast:
3	chrX:153236668..153238207-chrX:153597097..153599855,3	MCF-7	breast:
4	chrX:153266208..153269138-chrX:153597364..153599316,2	K562	blood:
5	chrX:153598203..153601789-chrX:153761157..153765642,8	MCF-7	breast:
6	chr11:63993654..63994276-chrX:153598283..153599129,2	Hela-S3	cervix:
7	chrX:153596758..153603302-chrX:153757517..153765995,15	MCF-7	breast:
8	chr17:60004432..60006975-chrX:153598237..153599773,2	MCF-7	breast:
9	chrX:153560347..153562674-chrX:153597012..153599559,3	K562	blood:
10	chrX:153597771..153599703-chrX:153989259..153992360,3	K562	blood:
11	chrX:153597566..153600681-chrX:153636229..153641525,5	K562	blood:
12	chrX:153597145..153602460-chrX:153684166..153689341,12	MCF-7	breast:
13	chr8:128747244..128749911-chrX:153597954..153599772,2	MCF-7	breast:
14	chrX:153596589..153600122-chrX:153663177..153666593,6	K562	blood:
15	chrX:153555091..153558039-chrX:153596602..153598936,2	MCF-7	breast:
16	chrX:153597323..153599953-chrX:153767551..153771879,5	K562	blood:
17	chrX:153598177..153599749-chrX:153774215..153776821,2	K562	blood:
18	chrX:153594250..153603496-chrX:153624447..153635089,39	K562	blood:
19	chrX:153597323..153603501-chrX:153767536..153771485,7	K562	blood:
20	chr19:2093950..2096627-chrX:153598223..153600248,2	MCF-7	breast:
21	chrX:153598329..153600777-chrX:153686230..153689521,3	MCF-7	breast:
22	chrX:153595797..153602112-chrX:153766071..153771136,12	MCF-7	breast:
23	chrX:153595771..153598554-chrX:153758917..153761035,2	K562	blood:
24	chrX:153596732..153598578-chrX:153758288..153760053,2	MCF-7	breast:
25	chrX:153598236..153601152-chrX:153668310..153670441,2	MCF-7	breast:
26	chrX:153596666..153604722-chrX:153634859..153642638,15	MCF-7	breast:
27	chrX:153597195..153601946-chrX:153697915..153702072,4	MCF-7	breast:
28	chrX:153596460..153601893-chrX:153713560..153721410,16	MCF-7	breast:
29	chrX:153597126..153599527-chrX:153735372..153738267,3	K562	blood:
30	chrX:153598083..153601598-chrX:153742945..153745309,4	K562	blood:
31	chrX:153595922..153599079-chrX:153761912..153767346,5	K562	blood:
32	chrX:153550633..153555849-chrX:153596435..153601807,5	K562	blood:
33	chrX:153597634..153602392-chrX:153694750..153697416,5	K562	blood:
34	chrX:153236665..153239480-chrX:153596620..153599715,3	K562	blood:
35	chrX:153057548..153061045-chrX:153596083..153599292,3	MCF-7	breast:
36	chrX:153598108..153600933-chrX:153742821..153746218,3	MCF-7	breast:
37	chrX:153597515..153599538-chrX:153685497..153687791,2	K562	blood:
38	chrX:153551880..153553532-chrX:153597731..153599347,2	MCF-7	breast:
39	chrX:153592401..153602834-chrX:153624077..153632705,30	K562	blood:
40	chrX:153597589..153599547-chrX:153820994..153822865,2	MCF-7	breast:
41	chrX:153596642..153600094-chrX:153690004..153694161,3	K562	blood:
42	chrX:153595658..153604095-chrX:153765725..153780258,40	MCF-7	breast:
43	chrX:153598041..153598880-chrX:153629019..153629749,2	Hela-S3	cervix:
44	chrX:153595264..153612826-chrX:153621461..153634267,75	MCF-7	breast:
45	chrX:153596623..153600423-chrX:153670975..153673649,4	K562	blood:
46	chr9:98273303..98273822-chrX:153598030..153598632,2	NB4	blood:
47	chr17:57914815..57916522-chrX:153597263..153599705,2	MCF-7	breast:
48	chrX:153597681..153599817-chrX:153742419..153745100,3	MCF-7	breast:
49	chrX:153596552..153604370-chrX:153654056..153661278,16	MCF-7	breast:
50	chr1:150336506..150337490-chrX:153598276..153598963,2	Hela-S3	cervix:

Variant related genes	Relation type
FLNA	TF binding region
ENSG00000149761	Chromatin interaction
ENSG00000172534	Chromatin interaction
ENSG00000067829	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000143153	Chromatin interaction
ENSG00000163125	Chromatin interaction
ENSG00000172081	Chromatin interaction
ENSG00000007350	Chromatin interaction
ENSG00000089820	Chromatin interaction
ENSG00000071553	Chromatin interaction
ENSG00000237707	Chromatin interaction
ENSG00000177854	Chromatin interaction
ENSG00000071889	Chromatin interaction
ENSG00000196976	Chromatin interaction
ENSG00000136997	Chromatin interaction
ENSG00000102178	Chromatin interaction
ENSG00000203879	Chromatin interaction
ENSG00000130827	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000099840	Chromatin interaction
ENSG00000120925	Chromatin interaction
ENSG00000013563	Chromatin interaction
ENSG00000126903	Chromatin interaction
ENSG00000130826	Chromatin interaction
ENSG00000071859	Chromatin interaction
ENSG00000180879	Chromatin interaction
ENSG00000147403	Chromatin interaction
ENSG00000108506	Chromatin interaction
ENSG00000073009	Chromatin interaction
ENSG00000207165	Chromatin interaction
ENSG00000102125	Chromatin interaction
ENSG00000197180	Chromatin interaction
ENSG00000168172	Chromatin interaction
ENSG00000160211	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs12007167	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs17426	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17428	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap]
rs2070816	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs2070822	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs2872817	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs4446899	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap]
rs4898478	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4898479	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5945185	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs5945413	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs5945423	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs915943	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv531228	chrX:152864376-153609161	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv531227	chrX:152864376-153655730	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
3	esv33199	chrX:152864376-153820241	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	276 gene(s)	inside rSNPs	diseases
4	nsv528291	chrX:152864376-153827637	Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription 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	277 gene(s)	inside rSNPs	diseases
5	nsv932632	chrX:153333946-153623000	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
6	nsv531232	chrX:153333946-153626120	Genic enhancers Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv531233	chrX:153333946-153626120	Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv523072	chrX:153333946-153626738	Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
9	nsv915605	chrX:153333946-153783638	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
10	nsv519042	chrX:153348431-153829693	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
11	nsv532962	chrX:153564946-153870337	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
12	nsv9999	chrX:153567427-153621413	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
13	nsv532963	chrX:153576890-153822717	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	195 gene(s)	inside rSNPs	diseases
14	nsv817569	chrX:153592317-153634020	Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	151 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2239470	PLXNA3	cis	temporal cortex	BrainEAC
rs2239470	PLXNA3	cis	occipital cortex	BrainEAC
rs2239470	PLXNA3	cis	frontal cortex	BrainEAC
rs2239470	PLXNA3	cis	brain	BrainEAC

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:153576400-153599400	ZNF genes & repeats	Fetal Stomach	stomach
2	chrX:153576600-153598800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
3	chrX:153576600-153599800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chrX:153576800-153603600	ZNF genes & repeats	Fetal Brain Female	brain
5	chrX:153592200-153599400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
6	chrX:153594200-153598800	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
7	chrX:153595000-153600600	Active TSS	HSMMtube	muscle
8	chrX:153595600-153599000	Transcr. at gene 5' and 3'	A549	lung
9	chrX:153595600-153599600	Transcr. at gene 5' and 3'	NHLF	lung
10	chrX:153596400-153599600	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
11	chrX:153596400-153600800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chrX:153596600-153598600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chrX:153596600-153599000	Transcr. at gene 5' and 3'	Dnd41	blood
14	chrX:153596600-153600000	Active TSS	Thymus	Thymus
15	chrX:153596800-153598600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chrX:153596800-153599000	Active TSS	Right Atrium	heart
17	chrX:153596800-153600400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
18	chrX:153596800-153600400	Active TSS	GM12878-XiMat	blood
19	chrX:153596800-153600600	Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chrX:153596800-153601000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chrX:153596800-153601200	Active TSS	HSMM	muscle
22	chrX:153596800-153601600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chrX:153596800-153601600	Active TSS	Rectal Smooth Muscle	rectum
24	chrX:153596800-153602200	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chrX:153597000-153598600	Flanking Active TSS	Fetal Thymus	thymus
26	chrX:153597000-153598800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chrX:153597000-153600200	Active TSS	Primary T cells from cord blood	blood
28	chrX:153597000-153600400	Active TSS	Primary monocytes fromperipheralblood	blood
29	chrX:153597000-153600400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chrX:153597000-153600400	Active TSS	Brain Anterior Caudate	brain
31	chrX:153597000-153600400	Active TSS	Esophagus	oesophagus
32	chrX:153597000-153600400	Active TSS	HMEC	breast
33	chrX:153597000-153600600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chrX:153597000-153600600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chrX:153597000-153600600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chrX:153597000-153600600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chrX:153597000-153600600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chrX:153597000-153600600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chrX:153597000-153600600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chrX:153597000-153600600	Active TSS	NH-A	brain
41	chrX:153597000-153600600	Active TSS	NHDF-Ad	bronchial
42	chrX:153597000-153600800	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chrX:153597000-153600800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chrX:153597000-153601000	Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chrX:153597000-153601000	Active TSS	Left Ventricle	heart
46	chrX:153597000-153604000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
47	chrX:153597200-153600000	Active TSS	Fetal Kidney	kidney
48	chrX:153597200-153600200	Active TSS	Fetal Lung	lung
49	chrX:153597200-153600200	Active TSS	Small Intestine	intestine
50	chrX:153597200-153600400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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