Variant report

Variant	nsv531670
Chromosome Location	chr9:140637909-140730467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1742)
CpG islands
(count:3181)
Chromatin interactive
region (count:58)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:140641019-140641614	GM12878	blood:	n/a	chr9:140641502-140641509
2	ATF2	chr9:140639148-140639804	GM12878	blood:	n/a	n/a
3	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
4	ATF2	chr9:140653486-140653886	GM12878	blood:	n/a	n/a
5	ATF2	chr9:140656794-140657321	GM12878	blood:	n/a	n/a
6	ATF2	chr9:140655367-140655871	GM12878	blood:	n/a	n/a
7	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
8	ATF2	chr9:140651891-140652508	GM12878	blood:	n/a	n/a
9	ATF2	chr9:140653453-140654075	GM12878	blood:	n/a	n/a
10	ATF2	chr9:140655366-140655982	GM12878	blood:	n/a	n/a
11	ATF2	chr9:140639968-140640492	GM12878	blood:	n/a	n/a
12	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
13	ATF2	chr9:140641009-140641568	GM12878	blood:	n/a	chr9:140641502-140641509
14	ATF2	chr9:140656647-140657415	GM12878	blood:	n/a	n/a
15	ATF2	chr9:140639164-140639781	GM12878	blood:	n/a	n/a
16	BACH1	chr9:140640020-140640565	H1-hESC	embryonic stem cell:	n/a	chr9:140640362-140640376
17	BACH1	chr9:140640186-140640518	K562	blood:	n/a	chr9:140640362-140640376
18	BATF	chr9:140641136-140641560	GM12878	blood:	n/a	chr9:140641365-140641374
19	BATF	chr9:140655479-140655850	GM12878	blood:	n/a	n/a
20	BATF	chr9:140656857-140657244	GM12878	blood:	n/a	n/a
21	BATF	chr9:140641077-140641535	GM12878	blood:	n/a	chr9:140641365-140641374
22	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131
23	BATF	chr9:140710702-140711592	GM12878	blood:	n/a	chr9:140711120-140711131
24	BATF	chr9:140639922-140640464	GM12878	blood:	n/a	n/a
25	BATF	chr9:140639192-140639625	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:140653509-140653972	GM12878	blood:	n/a	chr9:140653758-140653767
27	BCL11A	chr9:140703488-140703846	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:140656803-140657323	GM12878	blood:	n/a	chr9:140657018-140657027
29	BCL11A	chr9:140639203-140639643	GM12878	blood:	n/a	chr9:140639398-140639407
30	BCL11A	chr9:140710826-140711435	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:140651977-140652398	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:140641106-140641493	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:140655419-140655822	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:140720112-140720348	GM12878	blood:	n/a	chr9:140720260-140720269
35	BCL11A	chr9:140641138-140641493	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:140652026-140652377	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:140674551-140675913	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:140656833-140657295	GM12878	blood:	n/a	chr9:140657018-140657027
39	BCL3	chr9:140702187-140702477	GM12878	blood:	n/a	n/a
40	BCL3	chr9:140674295-140674898	GM12878	blood:	n/a	n/a
41	BCL3	chr9:140699190-140700049	GM12878	blood:	n/a	n/a
42	BCL3	chr9:140675353-140676090	GM12878	blood:	n/a	n/a
43	BCL3	chr9:140674364-140675145	GM12878	blood:	n/a	n/a
44	BCL3	chr9:140674914-140675145	GM12878	blood:	n/a	n/a
45	BCL3	chr9:140699230-140700056	GM12878	blood:	n/a	n/a
46	BCL3	chr9:140676233-140676492	GM12878	blood:	n/a	n/a
47	BCL3	chr9:140675450-140675734	GM12878	blood:	n/a	n/a
48	BCL3	chr9:140707704-140708126	GM12878	blood:	n/a	n/a
49	BCL3	chr9:140675789-140676170	GM12878	blood:	n/a	n/a
50	BCL3	chr9:140707638-140708059	GM12878	blood:	n/a	n/a

(count:3181 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140647870-140647920	HCF	heart:	n/a
2	chr9:140683797-140683847	BJ	skin:	n/a
3	chr9:140703588-140703638	K562	blood:	n/a
4	chr9:140652685-140652735	RPTEC	kidney:	n/a
5	chr9:140675929-140675979	LNCaP	prostate:	n/a
6	chr9:140673936-140673986	GM12878	blood:	n/a
7	chr9:140716770-140716820	HepG2	liver:	n/a
8	chr9:140658436-140658486	HEEpiC	esophagus:	n/a
9	chr9:140708214-140708264	AG10803	skin:	n/a
10	chr9:140647870-140647920	HCF	heart:	n/a
11	chr9:140683797-140683847	BJ	skin:	n/a
12	chr9:140703588-140703638	K562	blood:	n/a
13	chr9:140652685-140652735	RPTEC	kidney:	n/a
14	chr9:140675929-140675979	LNCaP	prostate:	n/a
15	chr9:140673936-140673986	GM12878	blood:	n/a
16	chr9:140716770-140716820	HepG2	liver:	n/a
17	chr9:140658436-140658486	HEEpiC	esophagus:	n/a
18	chr9:140708214-140708264	AG10803	skin:	n/a
19	chr9:140675616-140675666	MCF10A-Er-Src	breast:	n/a
20	chr9:140683797-140683847	GM06990	blood:	n/a
21	chr9:140683527-140683577	SAEC	small airway:	n/a
22	chr9:140709558-140709608	SK-N-SH	brain:	n/a
23	chr9:140703637-140703687	SK-N-MC	brain:	n/a
24	chr9:140681206-140681256	ECC-1	luminal epithelium:	n/a
25	chr9:140707378-140707428	Caco-2	colon:	n/a
26	chr9:140676853-140676903	Hela-S3	cervix:	n/a
27	chr9:140725587-140725637	ovcar-3	ovarian:	n/a
28	chr9:140673936-140673986	GM06990	blood:	n/a
29	chr9:140678883-140678933	HEEpiC	esophagus:	n/a
30	chr9:140709558-140709608	HRCEpiC	kidney:	n/a
31	chr9:140671632-140671682	SKMC	muscle:	n/a
32	chr9:140728301-140728351	AG09309	skin:	n/a
33	chr9:140651049-140651099	MCF-7	breast:	n/a
34	chr9:140656200-140656250	GM12891	blood:	n/a
35	chr9:140676141-140676191	HCPEpiC	choroid plexus:	n/a
36	chr9:140656981-140657031	AG04449	skin:	fetal
37	chr9:140671200-140671250	SK-N-SH_RA	brain:	n/a
38	chr9:140683527-140683577	BJ	skin:	n/a
39	chr9:140730317-140730367	BE2_C	brain:	n/a
40	chr9:140687144-140687194	HCF	heart:	n/a
41	chr9:140656981-140657031	HAEpiC	amniotic membrane:	n/a
42	chr9:140652711-140652761	K562	blood:	n/a
43	chr9:140683527-140683577	Hela-S3	cervix:	n/a
44	chr9:140704398-140704448	ProgFib	skin:	n/a
45	chr9:140676141-140676191	SK-N-SH_RA	brain:	n/a
46	chr9:140684842-140684892	HepG2	liver:	n/a
47	chr9:140703588-140703638	BJ	skin:	n/a
48	chr9:140675616-140675666	GM19239	blood:	n/a
49	chr9:140671200-140671250	NHDF-neo	bronchial:	n/a
50	chr9:140714075-140714125	AG04450	lung:	fetal

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140634880..140636428-chr9:140652392..140655145,2	MCF-7	breast:
2	chr9:140656494..140658049-chr9:140665141..140666954,2	MCF-7	breast:
3	chr9:140648170..140652364-chr9:140652458..140655697,5	MCF-7	breast:
4	chr9:140718370..140720341-chr9:140724405..140727123,2	MCF-7	breast:
5	chr9:140667022..140668743-chr9:140670497..140672972,3	MCF-7	breast:
6	chr9:140567845..140570418-chr9:140651009..140653801,2	MCF-7	breast:
7	chr9:140639569..140641263-chr9:140644746..140647470,2	MCF-7	breast:
8	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
9	chr9:140675774..140679711-chr9:140680099..140683198,4	K562	blood:
10	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:
11	chr9:140701752..140704462-chr9:140707799..140711263,3	MCF-7	breast:
12	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
13	chr9:140649627..140652485-chr9:140655729..140657732,2	MCF-7	breast:
14	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
15	chr9:140656494..140658049-chr9:140665141..140666954,2	MCF-7	breast:
16	chr9:140512733..140514752-chr9:140658191..140660880,2	MCF-7	breast:
17	chr9:140645397..140647015-chr9:140648908..140650692,2	K562	blood:
18	chr9:140620032..140621601-chr9:140644743..140646680,2	K562	blood:
19	chr9:140706148..140709058-chr9:140712432..140716292,4	K562	blood:
20	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
21	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
22	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
23	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
24	chr9:140667645..140669335-chr9:140669650..140672274,2	K562	blood:
25	chr9:140589041..140590820-chr9:140640169..140641796,2	K562	blood:
26	chr9:140636490..140638088-chr9:140638645..140641455,2	MCF-7	breast:
27	chr9:140722366..140725361-chr9:140730961..140733725,2	MCF-7	breast:
28	chr9:140649627..140652485-chr9:140655729..140657732,2	MCF-7	breast:
29	chr9:140471636..140473213-chr9:140654801..140656439,2	MCF-7	breast:
30	chr9:140667022..140668743-chr9:140670497..140672972,3	MCF-7	breast:
31	chr9:140591766..140593331-chr9:140667353..140669493,2	K562	blood:
32	chr9:140645397..140647015-chr9:140648908..140650692,2	K562	blood:
33	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
34	chr9:140720745..140725244-chr9:140725368..140729857,4	K562	blood:
35	chr9:140639569..140641263-chr9:140644746..140647470,2	MCF-7	breast:
36	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
37	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
38	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
39	chr9:140637205..140639952-chr9:140640284..140643115,2	K562	blood:
40	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
41	chr9:140641621..140643809-chr9:140652826..140654596,2	MCF-7	breast:
42	chr9:140637728..140639474-chr9:140643254..140646123,2	K562	blood:
43	chr9:140499260..140502923-chr9:140667967..140671652,3	MCF-7	breast:
44	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
45	chr9:140642217..140645455-chr9:140646960..140649880,4	K562	blood:
46	chr9:140648145..140650901-chr9:140651290..140654289,3	K562	blood:
47	chr9:140447426..140450339-chr9:140645965..140648548,2	K562	blood:
48	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
49	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
50	chr9:140662415..140665334-chr9:140667330..140669473,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CACNA1B-4	chr9:140657474-140659224	NONHSAT135751
2	lnc-AL772363.1-5	chr9:140682117-140683139	NONHSAT135752
3	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
2	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924
3	EHMT1	hsa-miR-1	chr9:140730432-140730455

Variant related genes	Relation type
MIR602	TF binding region
EHMT1	TF binding region
ENSG00000255585	TF binding region
MIR602	CpG island
EHMT1	CpG island
ENSG00000255585	CpG island
ENSG00000207693	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000255585	chromatin interactions
ENSG00000181090	chromatin interactions

Extended variants
information (count: 4396 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:4396 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142727972	chr9:140637931-140637932	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375192869	chr9:140637973-140637974	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75421798	chr9:140637989-140637990	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544345305	chr9:140637990-140637991	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138108260	chr9:140638022-140638023	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529993515	chr9:140638026-140638027	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547362155	chr9:140638032-140638033	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116060838	chr9:140638045-140638046	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149535210	chr9:140638046-140638047	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs36112625	chr9:140638076-140638077	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373601794	chr9:140638126-140638127	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370529961	chr9:140638157-140638158	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373918501	chr9:140638159-140638160	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537168710	chr9:140638186-140638187	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185439668	chr9:140638193-140638194	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567257889	chr9:140638201-140638202	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs143132200	chr9:140638231-140638232	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs377665858	chr9:140638311-140638312	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs552890425	chr9:140638312-140638313	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs369709381	chr9:140638330-140638331	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs111985990	chr9:140638343-140638344	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs368418026	chr9:140638345-140638346	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs538516467	chr9:140638357-140638358	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs371587885	chr9:140638370-140638371	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs558732856	chr9:140638415-140638416	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1129767	chr9:140638416-140638417	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs149871742	chr9:140638422-140638423	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs189753830	chr9:140638449-140638450	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs143891279	chr9:140638453-140638454	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs148681026	chr9:140638457-140638458	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs1129768	chr9:140638461-140638462	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368011879	chr9:140638462-140638463	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574815586	chr9:140638473-140638474	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200076276	chr9:140638477-140638478	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs540617218	chr9:140638479-140638480	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs146711478	chr9:140638507-140638508	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs368995503	chr9:140638512-140638513	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140345462	chr9:140638521-140638522	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532880924	chr9:140638531-140638532	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11137198	chr9:140638534-140638535	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs563106329	chr9:140638589-140638590	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376511310	chr9:140638594-140638595	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4979643	chr9:140638607-140638608	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs368147369	chr9:140638630-140638631	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183964747	chr9:140638634-140638635	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71510839	chr9:140638675-140638676	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11370621	chr9:140638757-140638758	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201333680	chr9:140638758-140638759	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs397894065	chr9:140638767-140638768	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148235146	chr9:140638774-140638775	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:3642 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140573000-140638400	Weak transcription	Small Intestine	intestine
2	chr9:140598800-140649800	Weak transcription	Stomach Mucosa	stomach
3	chr9:140610800-140640000	Weak transcription	HUVEC	blood vessel
4	chr9:140619200-140651400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:140624800-140638000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr9:140624800-140638400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:140628400-140638200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr9:140629000-140638000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr9:140629000-140638200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr9:140629000-140640000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr9:140629200-140638000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr9:140629200-140639000	Weak transcription	Fetal Kidney	kidney
13	chr9:140629400-140640800	Weak transcription	NHDF-Ad	bronchial
14	chr9:140629600-140638200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr9:140629800-140639200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr9:140630000-140639000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr9:140630200-140639000	Weak transcription	K562	blood
18	chr9:140630400-140638000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:140630400-140639000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:140630400-140639200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:140630600-140638800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr9:140631400-140639400	Strong transcription	Primary T cells from cord blood	blood
23	chr9:140631600-140640200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr9:140632000-140640000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:140632200-140649000	Weak transcription	Osteobl	bone
26	chr9:140632600-140638000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr9:140632600-140640000	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr9:140633800-140643600	Strong transcription	Thymus	Thymus
29	chr9:140633800-140663000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr9:140634000-140639600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr9:140634000-140639600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr9:140634000-140640000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr9:140634000-140643600	Strong transcription	Fetal Intestine Small	intestine
34	chr9:140634000-140645600	Strong transcription	Fetal Intestine Large	intestine
35	chr9:140634200-140640000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:140634200-140646400	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr9:140634400-140640400	Strong transcription	Gastric	stomach
38	chr9:140634400-140649400	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr9:140634600-140638600	Strong transcription	Primary B cells from peripheral blood	blood
40	chr9:140634600-140639000	Weak transcription	A549	lung
41	chr9:140634600-140651400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:140634800-140638400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr9:140634800-140639400	Weak transcription	Fetal Brain Male	brain
44	chr9:140634800-140641600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:140634800-140643800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr9:140635000-140638000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:140635000-140638000	Weak transcription	Ovary	ovary
48	chr9:140635000-140638000	Weak transcription	NH-A	brain
49	chr9:140635000-140638400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr9:140635000-140638800	Weak transcription	Brain Cingulate Gyrus	brain

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