Variant report

Variant	nsv1006466
Chromosome Location	chr4:81888983-82009675
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1306)
CpG islands
(count:1344)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:81961256-81961506	K562	blood:	n/a	n/a
2	ARID3A	chr4:81991005-81991235	K562	blood:	n/a	n/a
3	ARID3A	chr4:81911136-81911417	K562	blood:	n/a	n/a
4	ATF2	chr4:81973068-81973831	GM12878	blood:	n/a	n/a
5	ATF2	chr4:81973138-81973799	GM12878	blood:	n/a	n/a
6	BACH1	chr4:81951756-81953065	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:81960506-81960766	GM12878	blood:	n/a	n/a
8	BATF	chr4:81973255-81973680	GM12878	blood:	n/a	chr4:81973545-81973554
9	BATF	chr4:81973172-81973875	GM12878	blood:	n/a	chr4:81973545-81973554
10	BCL11A	chr4:81973200-81973736	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:81973262-81973619	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:81924719-81925038	GM12878	blood:	n/a	n/a
13	BCL3	chr4:81973203-81973754	GM12878	blood:	n/a	n/a
14	BCL3	chr4:82005799-82006080	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:81973242-81973817	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:81973110-81973931	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:81990990-81991205	K562	blood:	n/a	n/a
18	BHLHE40	chr4:81981513-81981604	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:81973189-81973970	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:81924674-81925174	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:81911201-81911407	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:81993187-81993491	HepG2	liver:	n/a	chr4:81993327-81993338 chr4:81993326-81993339 chr4:81993326-81993337
23	CEBPB	chr4:81963855-81964107	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:81960470-81960810	MCF-7	breast:	n/a	chr4:81960659-81960670
25	CEBPB	chr4:81942580-81943087	MCF-7	breast:	n/a	chr4:81942830-81942843 chr4:81942830-81942843
26	CEBPB	chr4:81987127-81987282	H1-hESC	embryonic stem cell:	n/a	chr4:81987187-81987198 chr4:81987188-81987199
27	CEBPB	chr4:81960523-81960775	K562	blood:	n/a	chr4:81960659-81960670
28	CEBPB	chr4:81960552-81960797	A549	lung:	n/a	chr4:81960659-81960670
29	CEBPB	chr4:81973129-81973925	GM12878	blood:	n/a	chr4:81973394-81973406
30	CEBPB	chr4:82000708-82000860	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:81991005-81991283	K562	blood:	n/a	n/a
32	CEBPB	chr4:81898327-81898488	A549	lung:	n/a	chr4:81898363-81898376 chr4:81898413-81898426 chr4:81898363-81898374
33	CEBPB	chr4:81982546-81982853	HepG2	liver:	n/a	chr4:81982682-81982693
34	CEBPB	chr4:81960482-81960815	IMR90	lung:	n/a	chr4:81960659-81960670
35	CEBPB	chr4:81987076-81987329	HepG2	liver:	n/a	chr4:81987187-81987198 chr4:81987188-81987199
36	CEBPB	chr4:81960506-81960831	HepG2	liver:	n/a	chr4:81960659-81960670
37	CEBPB	chr4:81973309-81973638	GM12878	blood:	n/a	chr4:81973394-81973406
38	CEBPB	chr4:81990976-81991287	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:82007633-82007733	HepG2	liver:	n/a	chr4:82007666-82007677
40	CEBPB	chr4:81990954-81991250	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:81960515-81960825	H1-hESC	embryonic stem cell:	n/a	chr4:81960659-81960670
42	CEBPB	chr4:81990961-81991273	K562	blood:	n/a	n/a
43	CEBPB	chr4:81987072-81987325	K562	blood:	n/a	chr4:81987187-81987198 chr4:81987188-81987199
44	CEBPB	chr4:81990950-81991276	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:81960502-81960804	Hela-S3	cervix:	n/a	chr4:81960659-81960670
46	CEBPB	chr4:81942629-81943071	MCF-7	breast:	n/a	chr4:81942830-81942843 chr4:81942830-81942843
47	CHD1	chr4:81952342-81952631	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:81988642-81988709	GM12878	blood:	n/a	n/a
49	CHD2	chr4:81924608-81925265	GM12878	blood:	n/a	n/a
50	CTBP2	chr4:81951739-81953170	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:81951956-81952006	HEK293	kidney:	embryo
2	chr4:81955126-81955176	NHBE	bronchial:	n/a
3	chr4:81951956-81952006	HEK293	kidney:	embryo
4	chr4:81955126-81955176	NHBE	bronchial:	n/a
5	chr4:81952653-81952703	RPTEC	kidney:	n/a
6	chr4:81951951-81952001	HCT-116	colon:	n/a
7	chr4:81975265-81975315	GM19239	blood:	n/a
8	chr4:81951951-81952001	HCF	heart:	n/a
9	chr4:81951956-81952006	NHDF-neo	bronchial:	n/a
10	chr4:81951953-81952003	SK-N-SH_RA	brain:	n/a
11	chr4:81952024-81952074	GM06990	blood:	n/a
12	chr4:81951953-81952003	T-47D	breast:	n/a
13	chr4:81951953-81952003	GM19239	blood:	n/a
14	chr4:81951073-81951123	A549	lung:	n/a
15	chr4:81952593-81952643	AG04449	skin:	fetal
16	chr4:81951951-81952001	Caco-2	colon:	n/a
17	chr4:81951472-81951522	CMK	blood:	n/a
18	chr4:81991102-81991152	HAEpiC	amniotic membrane:	n/a
19	chr4:81955126-81955176	Caco-2	colon:	n/a
20	chr4:81951073-81951123	IMR90	lung:	fetal
21	chr4:81952653-81952703	ECC-1	luminal epithelium:	n/a
22	chr4:81975265-81975315	SK-N-MC	brain:	n/a
23	chr4:81951472-81951522	RPTEC	kidney:	n/a
24	chr4:81952593-81952643	GM12891	blood:	n/a
25	chr4:81951956-81952006	PFSK-1	brain:	n/a
26	chr4:81975265-81975315	Caco-2	colon:	n/a
27	chr4:81961493-81961543	AG04450	lung:	fetal
28	chr4:81955126-81955176	HCM	heart:	n/a
29	chr4:81950160-81950210	HRCEpiC	kidney:	n/a
30	chr4:81952593-81952643	AG04450	lung:	fetal
31	chr4:81952008-81952058	H1-hESC	embryonic stem cell:	embryo
32	chr4:81961493-81961543	GM12891	blood:	n/a
33	chr4:81951951-81952001	PFSK-1	brain:	n/a
34	chr4:81975265-81975315	ovcar-3	ovarian:	n/a
35	chr4:81991102-81991152	PANC-1	pancreas:	n/a
36	chr4:81953041-81953091	PrEC	prostate:	n/a
37	chr4:81953041-81953091	SKMC	muscle:	n/a
38	chr4:81953041-81953091	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:81951956-81952006	A549	lung:	n/a
40	chr4:81975265-81975315	HMEC	breast:	n/a
41	chr4:81951446-81951496	HepG2	liver:	n/a
42	chr4:81951472-81951522	HNPCEpiC	eye:	n/a
43	chr4:81948124-81948174	Caco-2	colon:	n/a
44	chr4:81955126-81955176	A549	lung:	n/a
45	chr4:81952330-81952380	GM12878	blood:	n/a
46	chr4:81952593-81952643	HEK293	kidney:	embryo
47	chr4:82005992-82006042	Hela-S3	cervix:	n/a
48	chr4:81951951-81952001	AG09309	skin:	n/a
49	chr4:81951446-81951496	K562	blood:	n/a
50	chr4:81991102-81991152	HCPEpiC	choroid plexus:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:79873114..79873664-chr4:81910812..81911504,2	K562	blood:
2	chr4:81286864..81287739-chr4:81972911..81973930,4	K562	blood:
3	chr4:81283380..81284379-chr4:81910732..81911711,4	MCF-7	breast:
4	chr4:81283608..81284439-chr4:81960869..81961835,3	MCF-7	breast:
5	chr4:81948165..81950015-chr4:81959647..81961556,2	K562	blood:
6	chr4:82005105..82005858-chr4:82181508..82182280,3	MCF-7	breast:
7	chr4:81286893..81287953-chr4:81910802..81911642,3	MCF-7	breast:
8	chr4:81910904..81911808-chr4:81961317..81961859,2	MCF-7	breast:
9	chr4:81282384..81283008-chr4:81973306..81973843,2	MCF-7	breast:
10	chr4:81955196..81958140-chr4:81960309..81962642,2	K562	blood:
11	chr4:81990998..81991602-chr4:82272501..82273357,5	MCF-7	breast:
12	chr4:81955196..81958140-chr4:81960309..81962642,2	K562	blood:
13	chr4:81990594..81991584-chr4:82181118..82182501,8	MCF-7	breast:
14	chr4:81974080..81976056-chr4:81981350..81983878,2	K562	blood:
15	chr4:81974556..81977423-chr4:81980691..81984332,3	K562	blood:
16	chr4:81282194..81283135-chr4:81910846..81911347,2	K562	blood:
17	chr4:81975637..81977540-chr4:81988307..81990192,2	K562	blood:
18	chr4:81283280..81284253-chr4:81960976..81961810,2	MCF-7	breast:
19	chr4:81540203..81541132-chr4:81973708..81974534,2	MCF-7	breast:
20	chr4:81282233..81282906-chr4:81970669..81971299,2	MCF-7	breast:
21	chr4:82005004..82005857-chr4:82272588..82273446,6	MCF-7	breast:
22	chr4:81942639..81943385-chr7:30269373..30270144,2	MCF-7	breast:
23	chr4:81967067..81968988-chr4:81975749..81977538,2	K562	blood:
24	chr4:81953825..81956176-chr4:81958029..81960138,2	MCF-7	breast:
25	chr4:81286788..81287763-chr4:81910772..81911418,5	MCF-7	breast:
26	chr4:82005126..82005787-chr4:82272560..82273161,2	MCF-7	breast:
27	chr4:81283592..81284206-chr4:81961033..81961793,2	K562	blood:
28	chr4:81286735..81287727-chr4:81973316..81974174,3	MCF-7	breast:
29	chr4:81974080..81976056-chr4:81981350..81983878,2	K562	blood:
30	chr4:81953825..81956176-chr4:81958029..81960138,2	MCF-7	breast:
31	chr4:81967067..81968988-chr4:81975749..81977538,2	K562	blood:
32	chr4:81282234..81283281-chr4:81960825..81961642,3	MCF-7	breast:
33	chr4:81975637..81977540-chr4:81988307..81990192,2	K562	blood:
34	chr4:81282233..81283176-chr4:81960486..81961821,6	MCF-7	breast:
35	chr4:81539992..81540886-chr4:81910834..81911713,5	MCF-7	breast:
36	chr4:81286710..81287784-chr4:81960924..81961852,5	MCF-7	breast:
37	chr4:81910904..81911808-chr4:81961317..81961859,2	MCF-7	breast:
38	chr4:81990984..81991561-chr4:83122784..83123414,2	K562	blood:
39	chr4:81948165..81950015-chr4:81959647..81961556,2	K562	blood:
40	chr4:81282246..81283120-chr4:81973336..81973855,3	MCF-7	breast:
41	chr4:79873242..79873800-chr4:81973211..81973738,2	MCF-7	breast:
42	chr4:81990848..81991586-chr4:82272501..82273236,3	K562	blood:
43	chr4:81286810..81287407-chr4:81960897..81961588,2	MCF-7	breast:
44	chr4:81974556..81977423-chr4:81980691..81984332,3	K562	blood:
45	chr4:81990624..81991565-chr4:82272517..82273470,4	MCF-7	breast:

No data

Variant related genes	Relation type
BMP3	TF binding region
BMP3	CpG island

Extended variants
information (count: 3257 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3257 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71596044	chr4:81889000-81889001	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs556309400	chr4:81889102-81889103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113277302	chr4:81889106-81889107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183417639	chr4:81889110-81889111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542554414	chr4:81889119-81889120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556067622	chr4:81889175-81889176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72866930	chr4:81894847-81894848	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs6831480	chr4:81894879-81894880	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558004629	chr4:81894882-81894883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560577412	chr4:81894894-81894895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532751172	chr4:81894935-81894936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116250573	chr4:81894937-81894938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151049880	chr4:81894948-81894949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139702313	chr4:81894969-81894970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192776168	chr4:81894970-81894971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184950966	chr4:81894976-81894977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4693767	chr4:81894986-81894987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs143581231	chr4:81895004-81895005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373403464	chr4:81895015-81895016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570693117	chr4:81895026-81895027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs80313837	chr4:81895034-81895035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187874181	chr4:81895038-81895039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192109406	chr4:81895052-81895053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116835117	chr4:81895124-81895125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184300467	chr4:81895170-81895171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189506438	chr4:81895249-81895250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540223500	chr4:81895252-81895253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554127344	chr4:81895264-81895265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577513852	chr4:81895270-81895271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11725468	chr4:81895274-81895275	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563113094	chr4:81895285-81895286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557829253	chr4:81895293-81895294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386676555	chr4:81895295-81895296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192406280	chr4:81895303-81895304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541970511	chr4:81895315-81895316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35722280	chr4:81895317-81895318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557410165	chr4:81895319-81895320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559977552	chr4:81895334-81895335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527368933	chr4:81895338-81895339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547121080	chr4:81895373-81895374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570403535	chr4:81895390-81895391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183740776	chr4:81895399-81895400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549630371	chr4:81895400-81895401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199668413	chr4:81895407-81895408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377337116	chr4:81895423-81895424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189511454	chr4:81895425-81895426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565016815	chr4:81895433-81895434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6849713	chr4:81895454-81895455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112266314	chr4:81895463-81895464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568503708	chr4:81895466-81895467	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Myelodysplastic syndrome	18508791	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81888400-81889000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:81888600-81889200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:81888800-81889000	Bivalent Enhancer	NHDF-Ad	bronchial
4	chr4:81894800-81895600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:81907200-81907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:81907600-81908200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:81908400-81908600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:81910400-81911200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:81910800-81914200	Enhancers	Primary B cells from cord blood	blood
10	chr4:81911000-81911200	Weak transcription	Fetal Kidney	kidney
11	chr4:81911000-81911600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:81911000-81911600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:81911000-81911600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr4:81911000-81911600	Enhancers	Colon Smooth Muscle	Colon
15	chr4:81911000-81912200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:81911000-81912400	Enhancers	Primary B cells from peripheral blood	blood
17	chr4:81911400-81911600	Enhancers	Fetal Kidney	kidney
18	chr4:81911400-81912200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:81911400-81912400	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:81911600-81912200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:81912000-81912400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:81914600-81915600	Enhancers	Fetal Intestine Large	intestine
23	chr4:81915200-81915600	Enhancers	Fetal Intestine Small	intestine
24	chr4:81921400-81922000	Enhancers	Rectal Smooth Muscle	rectum
25	chr4:81921800-81922600	Enhancers	Colon Smooth Muscle	Colon
26	chr4:81923000-81923200	Enhancers	Duodenum Mucosa	Duodenum
27	chr4:81923200-81924600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr4:81924000-81924600	Enhancers	GM12878-XiMat	blood
29	chr4:81924000-81925600	Enhancers	Primary B cells from cord blood	blood
30	chr4:81924000-81925600	Enhancers	Primary B cells from peripheral blood	blood
31	chr4:81924000-81925800	Enhancers	Fetal Intestine Large	intestine
32	chr4:81924000-81926200	Enhancers	Fetal Intestine Small	intestine
33	chr4:81924600-81925000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:81924600-81925000	Flanking Active TSS	GM12878-XiMat	blood
35	chr4:81924600-81925200	Enhancers	Fetal Heart	heart
36	chr4:81924600-81925400	Enhancers	Duodenum Mucosa	Duodenum
37	chr4:81924600-81926400	Enhancers	Brain Germinal Matrix	brain
38	chr4:81924800-81925000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:81924800-81925200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:81924800-81925200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr4:81924800-81925400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:81924800-81925600	Enhancers	Primary hematopoietic stem cells	blood
43	chr4:81925000-81925400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:81925000-81925400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr4:81925000-81925800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:81925000-81925800	Enhancers	GM12878-XiMat	blood
47	chr4:81925000-81928400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:81925800-81929600	Weak transcription	Fetal Intestine Large	intestine
49	chr4:81926200-81929200	Weak transcription	Fetal Intestine Small	intestine
50	chr4:81929200-81929400	Enhancers	Fetal Intestine Small	intestine

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