Variant report

Variant	nsv1024629
Chromosome Location	chr4:147987351-148277008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1446)
CpG islands
(count:611)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:148018195-148018506	HepG2	liver:	n/a	n/a
2	BACH1	chr4:147990290-147990406	K562	blood:	n/a	n/a
3	BACH1	chr4:148079665-148079864	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:148213946-148213985	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:148039806-148040055	GM12878	blood:	n/a	n/a
6	BATF	chr4:148060595-148060948	GM12878	blood:	n/a	n/a
7	BATF	chr4:148039751-148040028	GM12878	blood:	n/a	n/a
8	BATF	chr4:148016837-148017036	GM12878	blood:	n/a	n/a
9	BATF	chr4:148060608-148060952	GM12878	blood:	n/a	n/a
10	BATF	chr4:148031690-148031957	GM12878	blood:	n/a	n/a
11	BATF	chr4:148261839-148262240	GM12878	blood:	n/a	n/a
12	BATF	chr4:148261867-148262233	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:148119641-148119804	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr4:148261742-148262052	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:148119611-148119868	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr4:148261694-148262154	GM12878	blood:	n/a	n/a
17	CBX3	chr4:148261189-148262132	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:148186332-148186711	HCT-116	colon:	n/a	n/a
19	CBX3	chr4:148186333-148186658	HCT-116	colon:	n/a	n/a
20	CEBPB	chr4:148150470-148150491	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:148160321-148160621	IMR90	lung:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
22	CEBPB	chr4:148208741-148208953	Hela-S3	cervix:	n/a	chr4:148208811-148208822
23	CEBPB	chr4:148208747-148208933	A549	lung:	n/a	chr4:148208811-148208822
24	CEBPB	chr4:148074353-148074603	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:148124283-148124514	IMR90	lung:	n/a	chr4:148124413-148124424 chr4:148124378-148124389
26	CEBPB	chr4:148160379-148160672	HepG2	liver:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
27	CEBPB	chr4:148078831-148079105	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:148074327-148074627	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:148024548-148025196	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:148124251-148124537	HepG2	liver:	n/a	chr4:148124413-148124424 chr4:148124378-148124389
31	CEBPB	chr4:148206444-148206641	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:148148552-148148747	HepG2	liver:	n/a	chr4:148148573-148148584
33	CEBPB	chr4:148117825-148118026	HepG2	liver:	n/a	chr4:148117899-148117910
34	CEBPB	chr4:148160406-148160651	A549	lung:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
35	CEBPB	chr4:148024874-148024997	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:148122357-148122725	IMR90	lung:	n/a	chr4:148122533-148122544
37	CEBPB	chr4:148210339-148210586	HepG2	liver:	n/a	chr4:148210456-148210467
38	CEBPB	chr4:148161709-148161887	HepG2	liver:	n/a	chr4:148161823-148161836 chr4:148161824-148161835 chr4:148161823-148161836
39	CEBPB	chr4:148010735-148010911	H1-hESC	embryonic stem cell:	n/a	chr4:148010785-148010796 chr4:148010784-148010797
40	CEBPB	chr4:148122546-148122595	K562	blood:	n/a	n/a
41	CEBPB	chr4:148017847-148018453	IMR90	lung:	n/a	chr4:148018002-148018015 chr4:148018046-148018059
42	CEBPB	chr4:148272260-148273163	HCT-116	colon:	n/a	chr4:148272450-148272461
43	CEBPB	chr4:148124302-148124520	Hela-S3	cervix:	n/a	chr4:148124413-148124424 chr4:148124378-148124389
44	CEBPB	chr4:148272323-148272603	K562	blood:	n/a	chr4:148272450-148272461
45	CEBPB	chr4:148268040-148268290	HepG2	liver:	n/a	chr4:148268181-148268192
46	CEBPB	chr4:148113829-148114137	HepG2	liver:	n/a	chr4:148113972-148113983
47	CEBPB	chr4:148024669-148025127	A549	lung:	n/a	n/a
48	CEBPB	chr4:148074337-148074526	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:148010742-148010831	HepG2	liver:	n/a	chr4:148010785-148010796 chr4:148010784-148010797
50	CEBPB	chr4:148272310-148272570	HepG2	liver:	n/a	chr4:148272450-148272461

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148260510-148260560	HRCEpiC	kidney:	n/a
2	chr4:148260510-148260560	HRCEpiC	kidney:	n/a
3	chr4:148010893-148010943	MCF-7	breast:	n/a
4	chr4:148079717-148079767	AG04450	lung:	fetal
5	chr4:148017404-148017454	HRPEpiC	eye:	n/a
6	chr4:148079717-148079767	ovcar-3	ovarian:	n/a
7	chr4:148045888-148045938	GM12892	blood:	n/a
8	chr4:148233162-148233212	HCF	heart:	n/a
9	chr4:148260510-148260560	AG04450	lung:	fetal
10	chr4:148233162-148233212	SK-N-MC	brain:	n/a
11	chr4:148254941-148254991	Caco-2	colon:	n/a
12	chr4:148079717-148079767	H1-hESC	embryonic stem cell:	embryo
13	chr4:148260510-148260560	H1-hESC	embryonic stem cell:	embryo
14	chr4:148119477-148119527	MCF10A-Er-Src	breast:	n/a
15	chr4:148233162-148233212	NH-A	brain:	n/a
16	chr4:148017404-148017454	HUVEC	blood vessel:	n/a
17	chr4:148010893-148010943	GM12891	blood:	n/a
18	chr4:148039868-148039918	H1-hESC	embryonic stem cell:	embryo
19	chr4:148116386-148116436	HUVEC	blood vessel:	n/a
20	chr4:148116386-148116436	HRE	kidney:	n/a
21	chr4:148119477-148119527	SKMC	muscle:	n/a
22	chr4:148039868-148039918	HNPCEpiC	eye:	n/a
23	chr4:148233162-148233212	Hela-S3	cervix:	n/a
24	chr4:148233162-148233212	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:148039868-148039918	GM12891	blood:	n/a
26	chr4:148254941-148254991	H1-hESC	embryonic stem cell:	embryo
27	chr4:148079717-148079767	HEK293	kidney:	embryo
28	chr4:148119477-148119527	HCT-116	colon:	n/a
29	chr4:148116386-148116436	A549	lung:	n/a
30	chr4:148119477-148119527	Hela-S3	cervix:	n/a
31	chr4:148116386-148116436	BE2_C	brain:	n/a
32	chr4:148260510-148260560	NHBE	bronchial:	n/a
33	chr4:148039868-148039918	AoSMC	blood vessel:	n/a
34	chr4:148045888-148045938	AG04450	lung:	fetal
35	chr4:148079717-148079767	NHDF-neo	bronchial:	n/a
36	chr4:148017404-148017454	AG10803	skin:	n/a
37	chr4:148254941-148254991	MCF10A-Er-Src	breast:	n/a
38	chr4:148010893-148010943	HEEpiC	esophagus:	n/a
39	chr4:148233162-148233212	BJ	skin:	n/a
40	chr4:148017404-148017454	HEEpiC	esophagus:	n/a
41	chr4:148254941-148254991	GM12892	blood:	n/a
42	chr4:148010893-148010943	GM12878	blood:	n/a
43	chr4:148045888-148045938	MCF-7	breast:	n/a
44	chr4:148116386-148116436	SKMC	muscle:	n/a
45	chr4:148260510-148260560	AG10803	skin:	n/a
46	chr4:148254941-148254991	NHDF-neo	bronchial:	n/a
47	chr4:148116386-148116436	GM12891	blood:	n/a
48	chr4:148119477-148119527	MCF-7	breast:	n/a
49	chr4:148233162-148233212	NHDF-neo	bronchial:	n/a
50	chr4:148017404-148017454	NT2-D1	testis:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:148028252..148030817-chr4:148066832..148068338,2	MCF-7	breast:
2	chr4:147891557..147893991-chr4:148019262..148022234,2	K562	blood:
3	chr4:147997064..147999039-chr4:148001355..148005540,3	K562	blood:
4	chr4:147939974..147940929-chr4:148017718..148018845,5	MCF-7	breast:
5	chr4:147996508..147999039-chr4:148000264..148002855,2	K562	blood:
6	chr4:148272436..148274239-chr4:148281813..148283538,2	MCF-7	breast:
7	chr4:148028252..148030817-chr4:148066832..148068338,2	MCF-7	breast:
8	chr4:147939892..147940886-chr4:148017933..148018857,4	K562	blood:
9	chr4:147940120..147940905-chr4:148014962..148015896,2	MCF-7	breast:
10	chr4:147263518..147264744-chr4:148017893..148018774,4	K562	blood:
11	chr4:148018109..148018832-chr4:148511578..148512144,2	MCF-7	breast:
12	chr4:148069096..148070846-chr4:148073108..148075098,2	MCF-7	breast:
13	chr4:147939981..147941106-chr4:148014945..148015994,5	MCF-7	breast:
14	chr4:147997064..147999039-chr4:148001355..148005540,3	K562	blood:
15	chr12:54519933..54522634-chr4:148134863..148137147,2	MCF-7	breast:
16	chr4:148031854..148032569-chr4:148511175..148512068,3	MCF-7	breast:
17	chr4:147938835..147939664-chr4:148018151..148018826,2	MCF-7	breast:
18	chr4:148069096..148070846-chr4:148073108..148075098,2	MCF-7	breast:
19	chr4:148157546..148159164-chr4:148159658..148162438,2	K562	blood:
20	chr4:147939977..147940938-chr4:148015247..148015842,2	MCF-7	breast:
21	chr4:148167189..148168690-chr8:125868444..125870063,3	MCF-7	breast:
22	chr4:148081448..148083313-chr4:148510559..148512058,10	K562	blood:
23	chr4:148134867..148136847-chr4:148142304..148144965,2	MCF-7	breast:
24	chr4:148078667..148079597-chr4:148511157..148512035,4	MCF-7	breast:
25	chr4:148078475..148079202-chr4:148299618..148300406,2	MCF-7	breast:
26	chr4:148201722..148203853-chr4:148204436..148207128,2	K562	blood:
27	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:
28	chr4:148081823..148082362-chr4:148299859..148300742,2	MCF-7	breast:
29	chr4:148081746..148082739-chr4:148787692..148788240,2	K562	blood:
30	chr4:148201722..148203853-chr4:148204436..148207128,2	K562	blood:
31	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:
32	chr4:148160683..148161374-chr5:115362795..115363673,2	MCF-7	breast:
33	chr4:148031852..148032807-chr4:148511183..148512139,6	MCF-7	breast:
34	chr4:147996508..147999039-chr4:148000264..148002855,2	K562	blood:
35	chr4:148157546..148159164-chr4:148159658..148162438,2	K562	blood:
36	chr4:148167022..148169732-chr4:149288503..149290776,2	K562	blood:
37	chr4:148134867..148136847-chr4:148142304..148144965,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548g-5p	chr4:148265833-148265855	MIMAT0022722
hsa-miR-548g-3p	chr4:148265795-148265816	MIMAT0005912

No data

Variant related genes	Relation type
MIR548G	TF binding region
MIR548G	CpG island
ENSG00000255080	chromatin interactions
ENSG00000151623	chromatin interactions

Extended variants
information (count: 8380 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:8380 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184670445	chr4:147987358-147987359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563370013	chr4:147987395-147987396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554132225	chr4:147987481-147987482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80020893	chr4:147987489-147987490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189447967	chr4:147987542-147987543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558964847	chr4:147987576-147987577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150115710	chr4:147987577-147987578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548818106	chr4:147987610-147987611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372426118	chr4:147987647-147987648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568674359	chr4:147987668-147987669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531105119	chr4:147987695-147987696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200997577	chr4:147987742-147987743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550920511	chr4:147987750-147987751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180752737	chr4:147987786-147987787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74710870	chr4:147987790-147987791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539977015	chr4:147987796-147987797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374348771	chr4:147987841-147987842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553397602	chr4:147987849-147987850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566823983	chr4:147987862-147987863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201971358	chr4:147987953-147987954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569763437	chr4:147987955-147987956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71592494	chr4:147987956-147987957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570614976	chr4:147987957-147987958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574668898	chr4:147987958-147987959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79803798	chr4:147987978-147987979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10561742	chr4:147987980-147987981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185835279	chr4:147988018-147988019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554816182	chr4:147988024-147988025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373072011	chr4:147988042-147988043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191084998	chr4:147988044-147988045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543583926	chr4:147988069-147988070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556914632	chr4:147988133-147988134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370358081	chr4:147988135-147988136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34691914	chr4:147988136-147988137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34112031	chr4:147988150-147988151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200542723	chr4:147988151-147988152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201208333	chr4:147988152-147988153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6835455	chr4:147988237-147988238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs55806320	chr4:147988272-147988273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528457886	chr4:147988397-147988398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145538881	chr4:147988428-147988429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186575461	chr4:147988494-147988495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541481185	chr4:147988512-147988513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562383196	chr4:147988562-147988563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72947707	chr4:147988631-147988632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs55700451	chr4:147988665-147988666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551142439	chr4:147988684-147988685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571104664	chr4:147988693-147988694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533568755	chr4:147988698-147988699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576595926	chr4:147988713-147988714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147980600-147994200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:147989800-147990000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:147990200-147990400	Enhancers	Stomach Smooth Muscle	stomach
4	chr4:147993600-147994400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr4:147994200-147994800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr4:147994200-147998800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:147995600-147995800	Enhancers	Fetal Heart	heart
8	chr4:147995800-147997600	Weak transcription	Fetal Heart	heart
9	chr4:147997400-147997600	Enhancers	Left Ventricle	heart
10	chr4:147997400-147998200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr4:147997600-147997800	Enhancers	Right Ventricle	heart
12	chr4:147997600-147999200	Weak transcription	Left Ventricle	heart
13	chr4:147997600-147999600	Enhancers	Fetal Heart	heart
14	chr4:147998000-147998200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
15	chr4:147998200-147998400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr4:147998200-147998600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr4:147998200-147999200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr4:147998200-147999200	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr4:147998400-147999000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:147998400-147999000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr4:147998400-147999200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr4:147998600-147998800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr4:147998600-147999000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:147998600-147999200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:147998800-147999400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr4:147998800-148000200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr4:147998800-148001600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:147999000-148001600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr4:147999200-147999400	Enhancers	Lung	lung
30	chr4:147999200-147999400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr4:147999200-148000400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:147999200-148000400	Enhancers	Left Ventricle	heart
33	chr4:147999400-147999800	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr4:147999400-148000400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:147999400-148000400	Weak transcription	Lung	lung
36	chr4:147999400-148002800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:147999600-147999800	Flanking Active TSS	Fetal Heart	heart
38	chr4:147999600-148000200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr4:147999600-148000400	Enhancers	Right Ventricle	heart
40	chr4:147999800-148000000	Enhancers	Stomach Smooth Muscle	stomach
41	chr4:147999800-148000200	Enhancers	Fetal Heart	heart
42	chr4:147999800-148000400	Enhancers	Adipose Nuclei	Adipose
43	chr4:147999800-148000800	Enhancers	Placenta Amnion	Placenta Amnion
44	chr4:147999800-148001800	Enhancers	Brain Germinal Matrix	brain
45	chr4:148000000-148000400	Enhancers	Colon Smooth Muscle	Colon
46	chr4:148000000-148000400	Enhancers	Fetal Lung	lung
47	chr4:148000000-148000400	Enhancers	Ovary	ovary
48	chr4:148000000-148000400	Enhancers	Right Atrium	heart
49	chr4:148000000-148000400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr4:148000000-148000800	Flanking Active TSS	Stomach Smooth Muscle	stomach

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