Variant report

Variant	nsv880240
Chromosome Location	chr4:147905897-148032003
allele	n/a
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	ARID3A	chr4:148018195-148018506	HepG2	liver:	n/a	n/a
2	BACH1	chr4:147990290-147990406	K562	blood:	n/a	n/a
3	BACH1	chr4:147927497-147927695	K562	blood:	n/a	n/a
4	BATF	chr4:148031690-148031957	GM12878	blood:	n/a	n/a
5	BATF	chr4:148016837-148017036	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:147978765-147978955	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:147940324-147940542	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:148017847-148018453	IMR90	lung:	n/a	chr4:148018002-148018015 chr4:148018046-148018059
9	CEBPB	chr4:147975355-147976159	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:148017802-148018496	Hela-S3	cervix:	n/a	chr4:148018002-148018015 chr4:148018046-148018059
11	CEBPB	chr4:148022918-148023067	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:148024874-148024997	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:147962053-147962391	H1-hESC	embryonic stem cell:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
14	CEBPB	chr4:148029676-148029947	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:147999495-147999820	HepG2	liver:	n/a	chr4:147999658-147999667 chr4:147999656-147999667 chr4:147999657-147999668 chr4:147999656-147999669 chr4:147999656-147999669 chr4:147999658-147999667 chr4:147999658-147999667 chr4:147999658-147999667
16	CEBPB	chr4:148024626-148025135	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:147962036-147962406	IMR90	lung:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
18	CEBPB	chr4:148010735-148010911	H1-hESC	embryonic stem cell:	n/a	chr4:148010785-148010796 chr4:148010784-148010797
19	CEBPB	chr4:147971714-147972044	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:147938303-147938627	Hela-S3	cervix:	n/a	chr4:147938454-147938467
21	CEBPB	chr4:147962032-147962406	K562	blood:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
22	CEBPB	chr4:147962041-147962323	ECC-1	luminal epithelium:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
23	CEBPB	chr4:147962077-147962402	Hela-S3	cervix:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
24	CEBPB	chr4:148024548-148025196	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:147999549-147999830	IMR90	lung:	n/a	chr4:147999658-147999667 chr4:147999656-147999667 chr4:147999657-147999668 chr4:147999656-147999669 chr4:147999656-147999669 chr4:147999658-147999667 chr4:147999658-147999667 chr4:147999658-147999667
26	CEBPB	chr4:148010742-148010831	HepG2	liver:	n/a	chr4:148010785-148010796 chr4:148010784-148010797
27	CEBPB	chr4:147962026-147962304	A549	lung:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
28	CEBPB	chr4:148024669-148025127	A549	lung:	n/a	n/a
29	CEBPB	chr4:147962046-147962410	HepG2	liver:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
30	CEBPB	chr4:147962074-147962401	A549	lung:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
31	CEBPB	chr4:147962055-147962317	MCF-7	breast:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
32	CEBPB	chr4:147962069-147962278	ECC-1	luminal epithelium:	n/a	chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962216-147962225 chr4:147962214-147962227
33	CHD2	chr4:148024766-148025069	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr4:147940280-147940430	MCF-7	breast:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
35	CTCF	chr4:148015500-148015650	AG09309	skin:	n/a	chr4:148015531-148015549
36	CTCF	chr4:147940340-147940490	HUVEC	blood vessel:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
37	CTCF	chr4:147977800-147977950	AG09319	gingival:	n/a	n/a
38	CTCF	chr4:147940320-147940470	GM12870	blood:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
39	CTCF	chr4:147940640-147940790	GM12864	blood:	n/a	n/a
40	CTCF	chr4:147978240-147978390	AG10803	skin:	n/a	n/a
41	CTCF	chr4:147940340-147940490	GM12864	blood:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
42	CTCF	chr4:147940239-147940559	Spleen_OC	spleen:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
43	CTCF	chr4:147940300-147940450	HVMF	connective:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
44	CTCF	chr4:148015444-148015652	LNCaP	prostate:	n/a	chr4:148015531-148015549
45	CTCF	chr4:148018260-148018410	HMEC	breast:	n/a	chr4:148018353-148018369 chr4:148018347-148018368 chr4:148018352-148018370 chr4:148018357-148018365
46	CTCF	chr4:147940340-147940490	AoAF	blood vessel:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
47	CTCF	chr4:147940244-147940530	MCF-7	breast:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
48	CTCF	chr4:148015440-148015590	BJ	skin:	n/a	chr4:148015531-148015549
49	CTCF	chr4:147940320-147940470	HCFaa	heart:	n/a	chr4:147940394-147940407 chr4:147940391-147940409 chr4:147940393-147940414
50	CTCF	chr4:147926760-147926910	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148010893-148010943	IMR90	lung:	fetal
2	chr4:148010893-148010943	IMR90	lung:	fetal
3	chr4:147925275-147925325	Caco-2	colon:	n/a
4	chr4:148010893-148010943	NHDF-neo	bronchial:	n/a
5	chr4:148017404-148017454	GM06990	blood:	n/a
6	chr4:147925275-147925325	SK-N-SH_RA	brain:	n/a
7	chr4:148010893-148010943	SK-N-SH_RA	brain:	n/a
8	chr4:148010893-148010943	GM12891	blood:	n/a
9	chr4:147971312-147971362	HIPEpiC	eye:	n/a
10	chr4:147925275-147925325	H1-hESC	embryonic stem cell:	embryo
11	chr4:147983153-147983203	NHDF-neo	bronchial:	n/a
12	chr4:148010893-148010943	HUVEC	blood vessel:	n/a
13	chr4:147983153-147983203	SAEC	small airway:	n/a
14	chr4:147932916-147932966	ProgFib	skin:	n/a
15	chr4:147983153-147983203	T-47D	breast:	n/a
16	chr4:147983153-147983203	H1-hESC	embryonic stem cell:	embryo
17	chr4:147932916-147932966	GM12878	blood:	n/a
18	chr4:147932916-147932966	ovcar-3	ovarian:	n/a
19	chr4:148017404-148017454	AG04449	skin:	fetal
20	chr4:147983153-147983203	GM12892	blood:	n/a
21	chr4:147932916-147932966	Hela-S3	cervix:	n/a
22	chr4:147925275-147925325	HEEpiC	esophagus:	n/a
23	chr4:147932916-147932966	T-47D	breast:	n/a
24	chr4:147925275-147925325	AoSMC	blood vessel:	n/a
25	chr4:147983153-147983203	HCM	heart:	n/a
26	chr4:148017404-148017454	SAEC	small airway:	n/a
27	chr4:147971312-147971362	AG10803	skin:	n/a
28	chr4:147932916-147932966	LNCaP	prostate:	n/a
29	chr4:147983153-147983203	PrEC	prostate:	n/a
30	chr4:147983153-147983203	HL-60	blood:	n/a
31	chr4:147925275-147925325	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:148010893-148010943	Jurkat	blood:	n/a
33	chr4:147925275-147925325	BJ	skin:	n/a
34	chr4:148010893-148010943	ovcar-3	ovarian:	n/a
35	chr4:148017404-148017454	NH-A	brain:	n/a
36	chr4:147971312-147971362	PrEC	prostate:	n/a
37	chr4:147983153-147983203	PFSK-1	brain:	n/a
38	chr4:147932916-147932966	RPTEC	kidney:	n/a
39	chr4:148017404-148017454	NT2-D1	testis:	n/a
40	chr4:147971312-147971362	SKMC	muscle:	n/a
41	chr4:147932916-147932966	Hepatocyte	liver:	n/a
42	chr4:148010893-148010943	SK-N-SH	brain:	n/a
43	chr4:147971312-147971362	HAEpiC	amniotic membrane:	n/a
44	chr4:148010893-148010943	GM12892	blood:	n/a
45	chr4:147971312-147971362	ovcar-3	ovarian:	n/a
46	chr4:148010893-148010943	CMK	blood:	n/a
47	chr4:148010893-148010943	AG09319	gingival:	n/a
48	chr4:147925275-147925325	HL-60	blood:	n/a
49	chr4:148017404-148017454	Hela-S3	cervix:	n/a
50	chr4:148017404-148017454	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:147939977..147940938-chr4:148015247..148015842,2	MCF-7	breast:
2	chr4:147996508..147999039-chr4:148000264..148002855,2	K562	blood:
3	chr4:147263518..147264744-chr4:148017893..148018774,4	K562	blood:
4	chr4:147940120..147940905-chr4:148014962..148015896,2	MCF-7	breast:
5	chr4:148018109..148018832-chr4:148511578..148512144,2	MCF-7	breast:
6	chr4:147946922..147949325-chr4:147949441..147951136,2	K562	blood:
7	chr4:147939892..147940886-chr4:148017933..148018857,4	K562	blood:
8	chr4:148031852..148032807-chr4:148511183..148512139,6	MCF-7	breast:
9	chr4:147939981..147941106-chr4:148014945..148015994,5	MCF-7	breast:
10	chr4:147997064..147999039-chr4:148001355..148005540,3	K562	blood:
11	chr4:147939974..147940929-chr4:148017718..148018845,5	MCF-7	breast:
12	chr4:147997064..147999039-chr4:148001355..148005540,3	K562	blood:
13	chr4:147938835..147939664-chr4:148018151..148018826,2	MCF-7	breast:
14	chr4:147939970..147940883-chr4:148787667..148788628,4	K562	blood:
15	chr4:148031854..148032569-chr4:148511175..148512068,3	MCF-7	breast:
16	chr4:147939981..147941106-chr4:148014945..148015994,5	MCF-7	breast:
17	chr4:148028252..148030817-chr4:148066832..148068338,2	MCF-7	breast:
18	chr4:147891557..147893991-chr4:148019262..148022234,2	K562	blood:
19	chr4:147946196..147949325-chr4:147949429..147951136,3	K562	blood:
20	chr4:147939974..147940929-chr4:148017718..148018845,5	MCF-7	breast:
21	chr4:147946196..147949325-chr4:147949429..147951136,3	K562	blood:
22	chr4:147940120..147940905-chr4:148014962..148015896,2	MCF-7	breast:
23	chr4:147996508..147999039-chr4:148000264..148002855,2	K562	blood:
24	chr4:147938835..147939664-chr4:148018151..148018826,2	MCF-7	breast:
25	chr4:147946922..147949325-chr4:147949441..147951136,2	K562	blood:
26	chr4:147939977..147940938-chr4:148015247..148015842,2	MCF-7	breast:
27	chr4:147939892..147940886-chr4:148017933..148018857,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POU4F2-4	chr4:147926644-147930297	ENSG00000260090.1
2	lnc-POU4F2-5	chr4:147947073-147951224	NONHSAT098680

Variant related genes	Relation type
ENSG00000260090	TF binding region
ENSG00000260090	CpG island

Extended variants
information (count: 4411 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4411 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1347655	chr4:147905897-147905898	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145474902	chr4:147905902-147905903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563972239	chr4:147905929-147905930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116379296	chr4:147905938-147905939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542501796	chr4:147906003-147906004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562373811	chr4:147906012-147906013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180905202	chr4:147906024-147906025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528282178	chr4:147906035-147906036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185510827	chr4:147906036-147906037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567200962	chr4:147906044-147906045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140219287	chr4:147906049-147906050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143910607	chr4:147906050-147906051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566569075	chr4:147906053-147906054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529258017	chr4:147906058-147906059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375135901	chr4:147906070-147906071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548034077	chr4:147906090-147906091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568285607	chr4:147906117-147906118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146864168	chr4:147906120-147906121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552187880	chr4:147906123-147906124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376845351	chr4:147906137-147906138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570503308	chr4:147906157-147906158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34091904	chr4:147911826-147911827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557312532	chr4:147911848-147911849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1370303	chr4:147911890-147911891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568118233	chr4:147911899-147911900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537251493	chr4:147911905-147911906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550666870	chr4:147911932-147911933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570577356	chr4:147911943-147911944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539424607	chr4:147911947-147911948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143293522	chr4:147912002-147912003	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs72733758	chr4:147912003-147912004	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535736270	chr4:147912047-147912048	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs376785200	chr4:147912070-147912071	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs115662292	chr4:147912107-147912108	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs531907480	chr4:147912129-147912130	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs367805734	chr4:147912133-147912134	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs181581077	chr4:147912218-147912219	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564227869	chr4:147912241-147912242	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs28429124	chr4:147912247-147912248	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147890145	chr4:147912264-147912265	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs57807775	chr4:147912267-147912268	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs529295882	chr4:147912268-147912269	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs187000245	chr4:147912296-147912297	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs369157252	chr4:147912325-147912326	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs190813495	chr4:147912337-147912338	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs530584238	chr4:147912369-147912370	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs180815125	chr4:147912399-147912400	Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs570538840	chr4:147912437-147912438	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs539583688	chr4:147912489-147912490	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs546728222	chr4:147912493-147912494	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147905800-147906200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:147911800-147912000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:147912000-147912400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:147912000-147912600	ZNF genes & repeats	Pancreas	Pancrea
5	chr4:147912000-147913000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:147912400-147913200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:147912600-147913200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:147912800-147913000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:147912800-147913200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:147913400-147925200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:147919200-147919600	Enhancers	GM12878-XiMat	blood
12	chr4:147919200-147919800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:147923000-147926600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr4:147923400-147926000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:147923400-147926000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:147923600-147924000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:147923600-147924200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:147923600-147925000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr4:147923600-147925800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:147923600-147925800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:147924000-147925200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:147924200-147925200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:147925000-147925400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr4:147925200-147925800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr4:147925200-147926000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:147925200-147926000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:147925400-147925600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr4:147925600-147925800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:147925800-147926600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:147925800-147932600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:147925800-147932600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:147925800-147936600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:147926000-147927800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:147926000-147932200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr4:147926600-147926800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:147926600-147932600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr4:147926800-147932000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:147927800-147928200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:147927800-147930000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:147928200-147932200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr4:147930000-147932200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:147931000-147931200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:147931800-147933600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:147932000-147934400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:147932200-147932600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:147932200-147933000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:147932200-147933800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:147932200-147934400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:147932200-147934400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:147932400-147934000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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