Variant report

Variant	nsv949327
Chromosome Location	chr7:119179990-119402882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:61)
Chromatin interactive
region (count:66)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:119356600-119356718	K562	blood:	n/a	n/a
2	ATF1	chr7:119329630-119329700	K562	blood:	n/a	n/a
3	ATF1	chr7:119360724-119360869	K562	blood:	n/a	n/a
4	ATF2	chr7:119351098-119351553	GM12878	blood:	n/a	n/a
5	ATF2	chr7:119351112-119351541	GM12878	blood:	n/a	n/a
6	BACH1	chr7:119270769-119270846	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:119278105-119278207	K562	blood:	n/a	n/a
8	BATF	chr7:119351170-119351425	GM12878	blood:	n/a	chr7:119351322-119351330
9	BATF	chr7:119351259-119351432	GM12878	blood:	n/a	chr7:119351322-119351330
10	BATF	chr7:119321466-119321694	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:119351161-119351439	GM12878	blood:	n/a	chr7:119351318-119351327
12	BCL11A	chr7:119297324-119297552	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:119235049-119235354	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCLAF1	chr7:119351118-119351465	GM12878	blood:	n/a	chr7:119351318-119351327
15	CBX3	chr7:119334652-119334910	HCT-116	colon:	n/a	n/a
16	CBX3	chr7:119185151-119185664	HCT-116	colon:	n/a	n/a
17	CCNT2	chr7:119393741-119394095	K562	blood:	n/a	n/a
18	CCNT2	chr7:119201981-119202070	K562	blood:	n/a	n/a
19	CCNT2	chr7:119233909-119234326	K562	blood:	n/a	n/a
20	CEBPB	chr7:119254313-119254501	K562	blood:	n/a	chr7:119254401-119254414 chr7:119254403-119254414 chr7:119254403-119254414
21	CEBPB	chr7:119183182-119183277	K562	blood:	n/a	chr7:119183252-119183263
22	CEBPB	chr7:119303326-119303558	Hela-S3	cervix:	n/a	chr7:119303419-119303430
23	CEBPB	chr7:119268481-119268665	K562	blood:	n/a	n/a
24	CEBPB	chr7:119372074-119372417	A549	lung:	n/a	chr7:119372394-119372405
25	CEBPB	chr7:119358176-119358453	K562	blood:	n/a	chr7:119358303-119358314
26	CEBPB	chr7:119377515-119377814	IMR90	lung:	n/a	chr7:119377632-119377645
27	CEBPB	chr7:119398879-119398991	K562	blood:	n/a	n/a
28	CEBPB	chr7:119372061-119372477	HepG2	liver:	n/a	chr7:119372394-119372405
29	CEBPB	chr7:119360655-119360991	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:119183098-119183415	A549	lung:	n/a	chr7:119183252-119183263
31	CEBPB	chr7:119277538-119277743	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:119358226-119358455	HepG2	liver:	n/a	chr7:119358303-119358314
33	CEBPB	chr7:119369877-119370079	A549	lung:	n/a	n/a
34	CEBPB	chr7:119388624-119388839	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:119184919-119185504	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:119212161-119212254	A549	lung:	n/a	n/a
37	CEBPB	chr7:119201365-119201423	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:119304734-119305040	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:119358136-119358438	IMR90	lung:	n/a	chr7:119358303-119358314
40	CEBPB	chr7:119358170-119358424	A549	lung:	n/a	chr7:119358303-119358314
41	CEBPB	chr7:119402874-119403217	K562	blood:	n/a	chr7:119403043-119403054 chr7:119403045-119403056 chr7:119403043-119403056
42	CEBPB	chr7:119268502-119268702	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:119303361-119303556	HepG2	liver:	n/a	chr7:119303419-119303430
44	CEBPB	chr7:119371952-119372521	K562	blood:	n/a	chr7:119372394-119372405
45	CEBPB	chr7:119183092-119183422	HepG2	liver:	n/a	chr7:119183252-119183263
46	CEBPB	chr7:119303419-119303431	K562	blood:	n/a	chr7:119303419-119303430
47	CEBPB	chr7:119184879-119185640	A549	lung:	n/a	n/a
48	CEBPB	chr7:119303311-119303575	IMR90	lung:	n/a	chr7:119303419-119303430
49	CHD2	chr7:119344754-119344845	K562	blood:	n/a	n/a
50	CREB1	chr7:119351192-119351624	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119260946-119260996	CMK	blood:	n/a
2	chr7:119260946-119260996	HAEpiC	amniotic membrane:	n/a
3	chr7:119260946-119260996	ECC-1	luminal epithelium:	n/a
4	chr7:119260946-119260996	HEEpiC	esophagus:	n/a
5	chr7:119260946-119260996	BJ	skin:	n/a
6	chr7:119260946-119260996	GM12878	blood:	n/a
7	chr7:119260946-119260996	H1-hESC	embryonic stem cell:	embryo
8	chr7:119260946-119260996	AG10803	skin:	n/a
9	chr7:119260946-119260996	BE2_C	brain:	n/a
10	chr7:119260946-119260996	GM12892	blood:	n/a
11	chr7:119260946-119260996	AG09319	gingival:	n/a
12	chr7:119260946-119260996	AG04450	lung:	fetal
13	chr7:119260946-119260996	SK-N-SH_RA	brain:	n/a
14	chr7:119260946-119260996	K562	blood:	n/a
15	chr7:119260946-119260996	HRCEpiC	kidney:	n/a
16	chr7:119260946-119260996	NHBE	bronchial:	n/a
17	chr7:119260946-119260996	HUVEC	blood vessel:	n/a
18	chr7:119260946-119260996	NB4	blood:	n/a
19	chr7:119260946-119260996	PANC-1	pancreas:	n/a
20	chr7:119260946-119260996	AG09309	skin:	n/a
21	chr7:119260946-119260996	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:119260946-119260996	AG04449	skin:	fetal
23	chr7:119260946-119260996	SK-N-SH	brain:	n/a
24	chr7:119260946-119260996	HCPEpiC	choroid plexus:	n/a
25	chr7:119260946-119260996	MCF10A-Er-Src	breast:	n/a
26	chr7:119260946-119260996	NT2-D1	testis:	n/a
27	chr7:119260946-119260996	Hepatocyte	liver:	n/a
28	chr7:119260946-119260996	NHDF-neo	bronchial:	n/a
29	chr7:119260946-119260996	HRPEpiC	eye:	n/a
30	chr7:119260946-119260996	LNCaP	prostate:	n/a
31	chr7:119260946-119260996	HCT-116	colon:	n/a
32	chr7:119260946-119260996	T-47D	breast:	n/a
33	chr7:119260946-119260996	Caco-2	colon:	n/a
34	chr7:119260946-119260996	GM06990	blood:	n/a
35	chr7:119260946-119260996	PrEC	prostate:	n/a
36	chr7:119260946-119260996	AoSMC	blood vessel:	n/a
37	chr7:119260946-119260996	IMR90	lung:	fetal
38	chr7:119260946-119260996	SKMC	muscle:	n/a
39	chr7:119260946-119260996	HL-60	blood:	n/a
40	chr7:119260946-119260996	HRE	kidney:	n/a
41	chr7:119260946-119260996	HMEC	breast:	n/a
42	chr7:119260946-119260996	Hela-S3	cervix:	n/a
43	chr7:119260946-119260996	HepG2	liver:	n/a
44	chr7:119260946-119260996	RPTEC	kidney:	n/a
45	chr7:119260946-119260996	U87	brain:	n/a
46	chr7:119260946-119260996	HNPCEpiC	eye:	n/a
47	chr7:119260946-119260996	SK-N-MC	brain:	n/a
48	chr7:119260946-119260996	GM12891	blood:	n/a
49	chr7:119260946-119260996	NH-A	brain:	n/a
50	chr7:119260946-119260996	ovcar-3	ovarian:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:119364721..119367176-chr7:119381458..119383230,2	K562	blood:
2	chr7:119212184..119216632-chr7:119220970..119225768,5	K562	blood:
3	chr7:119383539..119386290-chr7:119392991..119394503,2	K562	blood:
4	chr7:119360959..119363712-chr7:119366753..119368692,2	K562	blood:
5	chr7:119308246..119310474-chr7:119311862..119317073,5	K562	blood:
6	chr7:119336359..119340346-chr7:119340435..119346652,6	K562	blood:
7	chr7:119356426..119358294-chr7:119363548..119365311,2	K562	blood:
8	chr7:119336359..119340346-chr7:119340435..119346652,6	K562	blood:
9	chr7:119267813..119270560-chr7:119277143..119281317,3	K562	blood:
10	chr7:119383218..119386091-chr7:119386979..119388711,2	K562	blood:
11	chr7:119364721..119367176-chr7:119381458..119383230,2	K562	blood:
12	chr7:119293573..119296446-chr7:119311017..119312558,2	K562	blood:
13	chr7:119360284..119363279-chr7:119373457..119376079,2	K562	blood:
14	chr7:119234213..119235745-chr7:119237438..119239172,2	K562	blood:
15	chr7:119211056..119214261-chr7:119214480..119218185,4	K562	blood:
16	chr7:119188506..119190356-chr7:119200793..119202933,2	K562	blood:
17	chr7:119348460..119350527-chr7:119352829..119355249,2	K562	blood:
18	chr7:119212184..119214604-chr7:119220970..119224685,3	K562	blood:
19	chr7:119383218..119386091-chr7:119386979..119388711,2	K562	blood:
20	chr7:119212184..119216632-chr7:119220970..119225768,5	K562	blood:
21	chr7:119374698..119376654-chr7:119378712..119381116,2	K562	blood:
22	chr7:119360959..119363712-chr7:119366753..119368692,2	K562	blood:
23	chr7:119374698..119376654-chr7:119378712..119381116,2	K562	blood:
24	chr7:119267813..119270560-chr7:119277143..119281317,3	K562	blood:
25	chr7:119293573..119296446-chr7:119311017..119312558,2	K562	blood:
26	chr7:119215904..119218529-chr7:119221309..119224669,3	K562	blood:
27	chr7:119202572..119205180-chr8:103798970..103800546,2	MCF-7	breast:
28	chr7:119368480..119370359-chr7:119372677..119374451,2	K562	blood:
29	chr7:119360284..119363279-chr7:119373457..119376079,2	K562	blood:
30	chr7:119325886..119327423-chr7:119329257..119332197,2	K562	blood:
31	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:
32	chr7:119370722..119372961-chr7:119382422..119384559,2	K562	blood:
33	chr7:119298777..119301979-chr7:119302560..119305123,3	K562	blood:
34	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
35	chr7:119397490..119400025-chr7:119421872..119424720,2	MCF-7	breast:
36	chr7:119356426..119358294-chr7:119363548..119365311,2	K562	blood:
37	chr7:119211056..119214261-chr7:119214480..119218185,4	K562	blood:
38	chr7:119402295..119404288-chr7:119404943..119407340,2	K562	blood:
39	chr7:119212184..119214604-chr7:119220970..119224685,3	K562	blood:
40	chr7:119378597..119381783-chr7:119382170..119385913,4	K562	blood:
41	chr7:119346390..119349043-chr7:119407382..119409874,2	K562	blood:
42	chr7:119234213..119235745-chr7:119237438..119239172,2	K562	blood:
43	chr7:119308246..119311748-chr7:119315573..119317458,3	K562	blood:
44	chr7:119184831..119187773-chr7:119262380..119264496,2	MCF-7	breast:
45	chr7:119298777..119301979-chr7:119302560..119305123,3	K562	blood:
46	chr7:119308246..119311748-chr7:119315573..119317458,3	K562	blood:
47	chr7:119188506..119190356-chr7:119200793..119202933,2	K562	blood:
48	chr7:119325886..119327423-chr7:119329257..119332197,2	K562	blood:
49	chr7:119356426..119358294-chr7:119362114..119365311,3	K562	blood:
50	chr7:119192825..119195698-chr7:119199166..119201397,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCND2-3	chr7:119264815-119264891	NONHSAT122983
2	lnc-KCND2-3	chr7:119259423-119260624	NONHSAT122983
3	lnc-KCND2-2	chr7:119348262-119348369	NONHSAT122985
4	lnc-KCND2-2	chr7:119344514-119347011	NONHSAT122985
5	lnc-TSPAN12-8	chr7:119322820-119322866	NONHSAT122984
6	lnc-TSPAN12-4	chr7:119390869-119392229	XLOC_006580
7	lnc-TSPAN12-4	chr7:119344610-119345026	XLOC_006580
8	lnc-TSPAN12-8	chr7:119321046-119322265	NONHSAT122984

No data

Variant related genes	Relation type
ENSG00000256882	TF binding region
ENSG00000256882	CpG island
ENSG00000105258	chromatin interactions
ENSG00000105254	chromatin interactions
PDE12	miRNA target sites

Extended variants
information (count: 3611 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3611 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112203278	chr7:119183032-119183033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531761939	chr7:119183043-119183044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73719926	chr7:119183093-119183094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568374444	chr7:119183124-119183125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111722038	chr7:119183131-119183132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547707585	chr7:119183151-119183152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570676813	chr7:119183190-119183191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566144351	chr7:119183264-119183265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539631175	chr7:119183321-119183322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370232139	chr7:119183341-119183342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557596544	chr7:119183342-119183343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575288401	chr7:119183346-119183347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537552850	chr7:119183355-119183356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184114621	chr7:119183380-119183381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574369508	chr7:119183390-119183391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185847565	chr7:119183433-119183434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560461185	chr7:119183497-119183498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189768388	chr7:119183498-119183499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368622967	chr7:119183502-119183503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115728401	chr7:119183548-119183549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10268258	chr7:119183554-119183555	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576181347	chr7:119184218-119184219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558829513	chr7:119184219-119184220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148619612	chr7:119184287-119184288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562026353	chr7:119184327-119184328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527809701	chr7:119184385-119184386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6971212	chr7:119184389-119184390	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs564149476	chr7:119184397-119184398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191951869	chr7:119184416-119184417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550228812	chr7:119184429-119184430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183229677	chr7:119184434-119184435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529449385	chr7:119184483-119184484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549580728	chr7:119184491-119184492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568160160	chr7:119184493-119184494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533917611	chr7:119184507-119184508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553764706	chr7:119184569-119184570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570467302	chr7:119184609-119184610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539717540	chr7:119184666-119184667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556200802	chr7:119184684-119184685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77248663	chr7:119184686-119184687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576322367	chr7:119184723-119184724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115848231	chr7:119184735-119184736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111365997	chr7:119184753-119184754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572165262	chr7:119184755-119184756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541130493	chr7:119184759-119184760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564110876	chr7:119184789-119184790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79237039	chr7:119184811-119184812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73211836	chr7:119184885-119184886	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563804806	chr7:119184947-119184948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112851525	chr7:119184986-119184987	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119183000-119183600	Enhancers	Adipose Nuclei	Adipose
2	chr7:119184200-119186600	Enhancers	HUVEC	blood vessel
3	chr7:119184800-119186000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:119185200-119186000	Enhancers	A549	lung
5	chr7:119185400-119185800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:119185400-119185800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:119185400-119185800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:119185400-119186000	Enhancers	NH-A	brain
9	chr7:119185400-119186200	Enhancers	HMEC	breast
10	chr7:119185800-119186200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:119186200-119186600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:119206600-119206800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
13	chr7:119206600-119207200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:119206800-119207000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
15	chr7:119207000-119207200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
16	chr7:119212000-119213000	Enhancers	Brain Substantia Nigra	brain
17	chr7:119212200-119212800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:119212600-119213000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:119213000-119218200	Weak transcription	Brain Substantia Nigra	brain
20	chr7:119217400-119219000	Enhancers	Brain Hippocampus Middle	brain
21	chr7:119218200-119219000	Enhancers	Brain Substantia Nigra	brain
22	chr7:119233800-119235800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:119234000-119235600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:119234000-119235600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:119234000-119236400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr7:119234200-119235600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:119234600-119235200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr7:119234600-119235600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr7:119234600-119235800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:119234600-119235800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:119234600-119235800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:119234600-119236200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr7:119234800-119236400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:119235600-119236200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:119254400-119254600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:119254600-119257000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:119257000-119257200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:119257000-119257400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:119257200-119257400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:119257400-119259800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:119259800-119262000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:119260800-119261400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:119260800-119261800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:119261000-119261400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:119261000-119261400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:119261000-119261600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr7:119261000-119261600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:119261000-119261600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr7:119261200-119261400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr7:119261400-119261600	Enhancers	HUES48 Cell Line	embryonic stem cell

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