Variant report

Variant	nsv1004112
Chromosome Location	chr4:69284579-69410244
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	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
3	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
5	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
8	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
9	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
11	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:69300055-69300288	A549	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
13	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
14	CEBPB	chr4:69300028-69300381	IMR90	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
15	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
16	CEBPB	chr4:69300033-69300365	HepG2	liver:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
17	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:69300096-69300253	H1-hESC	embryonic stem cell:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
19	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:69300021-69300356	K562	blood:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
21	CTCF	chr4:69364108-69364453	H1-hESC	embryonic stem cell:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
22	CTCF	chr4:69369311-69369425	GM12892	blood:	n/a	n/a
23	CTCF	chr4:69364240-69364390	AG09319	gingival:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
24	CTCF	chr4:69369320-69369470	HepG2	liver:	n/a	n/a
25	CTCF	chr4:69364204-69364436	T-47D	breast:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
26	CTCF	chr4:69364280-69364430	HRE	kidney:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
27	CTCF	chr4:69369275-69369430	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:69369324-69369379	GM19238	blood:	n/a	n/a
29	CTCF	chr4:69364240-69364390	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
30	CTCF	chr4:69364192-69364438	GM10266	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
31	CTCF	chr4:69364300-69364450	SAEC	small airway:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
32	CTCF	chr4:69364245-69364422	Fibrobl	skin:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
33	CTCF	chr4:69364240-69364390	Hela-S3	cervix:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
34	CTCF	chr4:69364220-69364370	GM12866	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
35	CTCF	chr4:69364220-69364370	GM12869	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
36	CTCF	chr4:69364128-69364481	ECC-1	luminal epithelium:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
37	CTCF	chr4:69369366-69369384	HepG2	liver:	n/a	n/a
38	CTCF	chr4:69364240-69364390	HAc	cerebellar:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
39	CTCF	chr4:69331880-69332030	HMEC	breast:	n/a	n/a
40	CTCF	chr4:69364033-69364752	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
41	CTCF	chr4:69363963-69363985	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:69364260-69364410	GM12875	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
43	CTCF	chr4:69364300-69364450	GM12867	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
44	CTCF	chr4:69364234-69364416	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
45	CTCF	chr4:69364193-69364448	GM13977	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
46	CTCF	chr4:69364090-69364547	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69364300-69364450	GM12868	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69364180-69364330	HCT-116	colon:	n/a	chr4:69364310-69364328 chr4:69364311-69364327
49	CTCF	chr4:69384740-69384890	HMEC	breast:	n/a	n/a
50	CTCF	chr4:69364220-69364370	HepG2	liver:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69312514-69312564	A549	lung:	n/a
2	chr4:69312514-69312564	GM12878	blood:	n/a
3	chr4:69312514-69312564	AG09309	skin:	n/a
4	chr4:69312104-69312154	AoSMC	blood vessel:	n/a
5	chr4:69312514-69312564	SK-N-SH	brain:	n/a
6	chr4:69340916-69340966	NHBE	bronchial:	n/a
7	chr4:69340916-69340966	Hela-S3	cervix:	n/a
8	chr4:69313197-69313247	AoSMC	blood vessel:	n/a
9	chr4:69312514-69312564	MCF10A-Er-Src	breast:	n/a
10	chr4:69340916-69340966	MCF-7	breast:	n/a
11	chr4:69312514-69312564	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:69313197-69313247	NHBE	bronchial:	n/a
13	chr4:69355121-69355171	SK-N-SH	brain:	n/a
14	chr4:69312104-69312154	ECC-1	luminal epithelium:	n/a
15	chr4:69381368-69381418	RPTEC	kidney:	n/a
16	chr4:69312104-69312154	SKMC	muscle:	n/a
17	chr4:69355121-69355171	HepG2	liver:	n/a
18	chr4:69312104-69312154	GM12878	blood:	n/a
19	chr4:69381368-69381418	AG04449	skin:	fetal
20	chr4:69381368-69381418	HRE	kidney:	n/a
21	chr4:69313197-69313247	CMK	blood:	n/a
22	chr4:69355121-69355171	Hela-S3	cervix:	n/a
23	chr4:69313197-69313247	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:69381368-69381418	NB4	blood:	n/a
25	chr4:69355121-69355171	HCM	heart:	n/a
26	chr4:69312104-69312154	Jurkat	blood:	n/a
27	chr4:69340916-69340966	ProgFib	skin:	n/a
28	chr4:69312514-69312564	SAEC	small airway:	n/a
29	chr4:69340916-69340966	MCF10A-Er-Src	breast:	n/a
30	chr4:69313197-69313247	SK-N-MC	brain:	n/a
31	chr4:69312514-69312564	Hepatocyte	liver:	n/a
32	chr4:69355121-69355171	K562	blood:	n/a
33	chr4:69312514-69312564	NH-A	brain:	n/a
34	chr4:69355121-69355171	NB4	blood:	n/a
35	chr4:69340916-69340966	Jurkat	blood:	n/a
36	chr4:69340916-69340966	HCM	heart:	n/a
37	chr4:69381368-69381418	MCF-7	breast:	n/a
38	chr4:69312104-69312154	HL-60	blood:	n/a
39	chr4:69381368-69381418	PFSK-1	brain:	n/a
40	chr4:69340916-69340966	LNCaP	prostate:	n/a
41	chr4:69313197-69313247	HCM	heart:	n/a
42	chr4:69355121-69355171	HRE	kidney:	n/a
43	chr4:69355121-69355171	AoSMC	blood vessel:	n/a
44	chr4:69381368-69381418	ProgFib	skin:	n/a
45	chr4:69312514-69312564	HAEpiC	amniotic membrane:	n/a
46	chr4:69381368-69381418	HRPEpiC	eye:	n/a
47	chr4:69355121-69355171	T-47D	breast:	n/a
48	chr4:69312104-69312154	ovcar-3	ovarian:	n/a
49	chr4:69312104-69312154	K562	blood:	n/a
50	chr4:69381368-69381418	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
2	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
3	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
4	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
5	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
6	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
7	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
8	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
9	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
10	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
11	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
12	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
13	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
14	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
15	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
16	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
17	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
18	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
19	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
20	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
2	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733

Variant related genes	Relation type
TMPRSS11E	TF binding region
UGT2B29P	TF binding region
TMPRSS11E	CpG island
UGT2B29P	CpG island
ENSG00000083896	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000272626	chromatin interactions

Extended variants
information (count: 3889 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3889 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543306068	chr4:69284589-69284590	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs58500579	chr4:69284599-69284600	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs545655118	chr4:69284613-69284614	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191577447	chr4:69284628-69284629	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149708942	chr4:69284634-69284635	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554730419	chr4:69284646-69284647	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528699213	chr4:69284652-69284653	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145764066	chr4:69284693-69284694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs60942202	chr4:69284750-69284751	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59586015	chr4:69284771-69284772	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146557688	chr4:69284787-69284788	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141197151	chr4:69284791-69284792	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552405809	chr4:69284794-69284795	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181493106	chr4:69284806-69284807	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143404932	chr4:69284826-69284827	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554120688	chr4:69284828-69284829	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574129432	chr4:69284837-69284838	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35224077	chr4:69284840-69284841	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556802323	chr4:69284859-69284860	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112186704	chr4:69284881-69284882	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574580293	chr4:69284893-69284894	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576534028	chr4:69284897-69284898	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545282550	chr4:69284902-69284903	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560467331	chr4:69284907-69284908	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569930071	chr4:69284918-69284919	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572774990	chr4:69285022-69285023	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186970743	chr4:69285023-69285024	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190920649	chr4:69285064-69285065	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530059787	chr4:69285092-69285093	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58870478	chr4:69285093-69285094	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs150443225	chr4:69285117-69285118	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183444972	chr4:69285163-69285164	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188026437	chr4:69285181-69285182	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565566042	chr4:69285185-69285186	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551028810	chr4:69285186-69285187	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534589709	chr4:69285187-69285188	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548095264	chr4:69285201-69285202	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34458313	chr4:69285239-69285240	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536646859	chr4:69285270-69285271	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189754095	chr4:69285328-69285329	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183016834	chr4:69285334-69285335	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142772543	chr4:69285362-69285363	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543889546	chr4:69285371-69285372	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559175916	chr4:69285436-69285437	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572714175	chr4:69285588-69285589	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187824864	chr4:69285613-69285614	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372982166	chr4:69285614-69285615	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574732754	chr4:69285638-69285639	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370635876	chr4:69285662-69285663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543441732	chr4:69285679-69285680	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	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
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69276800-69284600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:69280000-69286000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:69280800-69289600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:69283400-69288000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr4:69283400-69288000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr4:69284200-69285000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr4:69284600-69287000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr4:69284600-69288000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:69285000-69287800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr4:69285000-69288000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr4:69285400-69286800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
12	chr4:69285600-69286000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:69286000-69286400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:69286000-69286400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:69286000-69287400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
16	chr4:69287000-69288000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr4:69288000-69291600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:69291600-69292400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:69292000-69292200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:69292800-69293200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:69293000-69295800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr4:69295600-69296000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:69295800-69296600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:69295800-69296600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:69296000-69296400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:69296000-69296400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:69296000-69296600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:69296400-69300400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr4:69296400-69300600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:69296600-69312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:69298200-69298800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr4:69298800-69300400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr4:69299400-69299600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:69299400-69299800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr4:69299800-69300200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:69300200-69303400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr4:69300400-69301000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:69300400-69301800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:69300400-69302800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr4:69300400-69303400	Enhancers	Primary T cells from cord blood	blood
41	chr4:69300400-69303400	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr4:69300400-69303400	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr4:69300600-69300800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:69300600-69300800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:69300600-69301000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:69300600-69302600	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr4:69300600-69302800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr4:69300600-69303400	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr4:69300600-69303400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr4:69300600-69303400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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