Variant report

Variant	nsv830017
Chromosome Location	chr4:98866299-99047777
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	chr4:99014048-99014354	HepG2	liver:	n/a	n/a
2	BCL3	chr4:98906959-98907234	GM12878	blood:	n/a	n/a
3	BCL3	chr4:98905816-98906082	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:98908240-98908390	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:99026262-99026519	IMR90	lung:	n/a	chr4:99026390-99026401
6	CEBPB	chr4:98898912-98899245	HepG2	liver:	n/a	chr4:98899094-98899105
7	CEBPB	chr4:98975792-98975954	HepG2	liver:	n/a	chr4:98975918-98975929
8	CEBPB	chr4:99026254-99026525	HepG2	liver:	n/a	chr4:99026390-99026401
9	CEBPB	chr4:98973085-98973241	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:99005909-99006159	IMR90	lung:	n/a	chr4:99006022-99006033
11	CEBPB	chr4:99026275-99026452	H1-hESC	embryonic stem cell:	n/a	chr4:99026390-99026401
12	CEBPB	chr4:99005881-99006191	HepG2	liver:	n/a	chr4:99006022-99006033
13	CEBPB	chr4:98989787-98989990	HepG2	liver:	n/a	chr4:98989872-98989883
14	CEBPB	chr4:98910863-98911031	A549	lung:	n/a	n/a
15	CEBPB	chr4:99005951-99006103	A549	lung:	n/a	chr4:99006022-99006033
16	CEBPB	chr4:98998918-98999191	HepG2	liver:	n/a	chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999041-98999052 chr4:98999040-98999051 chr4:98999042-98999051 chr4:98999040-98999053
17	CEBPB	chr4:98950612-98950807	HepG2	liver:	n/a	chr4:98950662-98950673
18	CEBPB	chr4:98999062-98999081	K562	blood:	n/a	n/a
19	CEBPB	chr4:99030855-99030922	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:98967948-98968326	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:99001733-99001756	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:98949000-98949150	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr4:98905808-98905935	HepG2	liver:	n/a	n/a
24	CTCF	chr4:99034301-99034425	GM10248	blood:	n/a	n/a
25	CTCF	chr4:99034212-99034532	IMR90	lung:	n/a	n/a
26	CTCF	chr4:99014120-99014270	GM12878	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
27	CTCF	chr4:98905920-98906070	HFF	foreskin:	n/a	n/a
28	CTCF	chr4:99034180-99034330	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr4:98905900-98906050	HCM	heart:	n/a	n/a
30	CTCF	chr4:98949080-98949230	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr4:99014120-99014270	GM12868	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
32	CTCF	chr4:98908320-98908470	AG04450	lung:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
33	CTCF	chr4:99034163-99034570	HCT-116	colon:	n/a	n/a
34	CTCF	chr4:98905860-98906010	NHEK	skin:	n/a	n/a
35	CTCF	chr4:98908300-98908450	GM12878	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
36	CTCF	chr4:98908279-98908433	Gliobla	brain:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
37	CTCF	chr4:98908280-98908430	GM12865	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
38	CTCF	chr4:98928140-98928290	GM12872	blood:	n/a	n/a
39	CTCF	chr4:98967872-98968147	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:98905780-98905930	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr4:99014120-99014270	HFF	foreskin:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
42	CTCF	chr4:98872311-98872378	GM20000	blood:	n/a	n/a
43	CTCF	chr4:99034360-99034510	HepG2	liver:	n/a	n/a
44	CTCF	chr4:98908277-98908493	Pancreas_OC	pancreas:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
45	CTCF	chr4:98905780-98905930	HPF	lung:	n/a	n/a
46	CTCF	chr4:99014100-99014250	HA-sp	spinal cord:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
47	CTCF	chr4:98949090-98949210	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:98949100-98949250	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:98949080-98949230	HCT-116	colon:	n/a	n/a
50	CTCF	chr4:98949100-98949226	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99008595-99008645	U87	brain:	n/a
2	chr4:99031533-99031583	U87	brain:	n/a
3	chr4:99008595-99008645	HAEpiC	amniotic membrane:	n/a
4	chr4:99008595-99008645	MCF-7	breast:	n/a
5	chr4:99008595-99008645	HEK293	kidney:	embryo
6	chr4:99031533-99031583	SKMC	muscle:	n/a
7	chr4:99008595-99008645	GM19239	blood:	n/a
8	chr4:99008595-99008645	AoSMC	blood vessel:	n/a
9	chr4:99008595-99008645	SK-N-SH	brain:	n/a
10	chr4:99031533-99031583	RPTEC	kidney:	n/a
11	chr4:99031533-99031583	MCF10A-Er-Src	breast:	n/a
12	chr4:99031533-99031583	A549	lung:	n/a
13	chr4:99031533-99031583	HRE	kidney:	n/a
14	chr4:99031533-99031583	HNPCEpiC	eye:	n/a
15	chr4:99008595-99008645	H1-hESC	embryonic stem cell:	embryo
16	chr4:99008595-99008645	PFSK-1	brain:	n/a
17	chr4:99031533-99031583	LNCaP	prostate:	n/a
18	chr4:99008595-99008645	SK-N-MC	brain:	n/a
19	chr4:99008595-99008645	HepG2	liver:	n/a
20	chr4:99008595-99008645	Hepatocyte	liver:	n/a
21	chr4:99031533-99031583	BE2_C	brain:	n/a
22	chr4:99031533-99031583	Jurkat	blood:	n/a
23	chr4:99031533-99031583	SK-N-SH_RA	brain:	n/a
24	chr4:99031533-99031583	HCPEpiC	choroid plexus:	n/a
25	chr4:99031533-99031583	HRPEpiC	eye:	n/a
26	chr4:99031533-99031583	ECC-1	luminal epithelium:	n/a
27	chr4:99008595-99008645	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:99008595-99008645	ECC-1	luminal epithelium:	n/a
29	chr4:99031533-99031583	HCM	heart:	n/a
30	chr4:99031533-99031583	HL-60	blood:	n/a
31	chr4:99031533-99031583	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:99008595-99008645	GM12892	blood:	n/a
33	chr4:99031533-99031583	Hela-S3	cervix:	n/a
34	chr4:99031533-99031583	BJ	skin:	n/a
35	chr4:99008595-99008645	RPTEC	kidney:	n/a
36	chr4:99031533-99031583	GM12891	blood:	n/a
37	chr4:99031533-99031583	HUVEC	blood vessel:	n/a
38	chr4:99008595-99008645	Hela-S3	cervix:	n/a
39	chr4:99031533-99031583	ProgFib	skin:	n/a
40	chr4:99031533-99031583	HEK293	kidney:	embryo
41	chr4:99008595-99008645	LNCaP	prostate:	n/a
42	chr4:99031533-99031583	H1-hESC	embryonic stem cell:	embryo
43	chr4:99008595-99008645	HUVEC	blood vessel:	n/a
44	chr4:99031533-99031583	NHDF-neo	bronchial:	n/a
45	chr4:99031533-99031583	AG10803	skin:	n/a
46	chr4:99008595-99008645	AG10803	skin:	n/a
47	chr4:99008595-99008645	ProgFib	skin:	n/a
48	chr4:99031533-99031583	AG09309	skin:	n/a
49	chr4:99008595-99008645	SKMC	muscle:	n/a
50	chr4:99008595-99008645	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
2	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
3	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
4	chr4:99001766..99003673-chr4:99063340..99066059,2	MCF-7	breast:
5	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
6	chr4:99012356..99014792-chr4:99062792..99064417,2	MCF-7	breast:
7	chr4:99033892..99034970-chr4:99063844..99064725,8	MCF-7	breast:
8	chr4:97404242..97405044-chr4:98905771..98906367,3	MCF-7	breast:
9	chr4:99034025..99034574-chr4:99308766..99309435,2	MCF-7	breast:
10	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
11	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
12	chr4:99037506..99039090-chr4:99060858..99063344,2	MCF-7	breast:
13	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
14	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
15	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
16	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-6	chr4:98969706-98970194	NONHSAT097481

Variant related genes	Relation type
STPG2	TF binding region
RPL5P12	TF binding region
DUTP8	TF binding region
STPG2	CpG island
RPL5P12	CpG island
DUTP8	CpG island
ENSG00000163116	chromatin interactions

Extended variants
information (count: 1995 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1995 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575808904	chr4:98866304-98866305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186677798	chr4:98866307-98866308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151309845	chr4:98866320-98866321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190734947	chr4:98866323-98866324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572637258	chr4:98866331-98866332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546408190	chr4:98866336-98866337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183108769	chr4:98866354-98866355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187751054	chr4:98866361-98866362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564628678	chr4:98866382-98866383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570933059	chr4:98866396-98866397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543910676	chr4:98866397-98866398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562195163	chr4:98866447-98866448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113852034	chr4:98866506-98866507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529685669	chr4:98866542-98866543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541448461	chr4:98866546-98866547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6843777	chr4:98866635-98866636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs527569546	chr4:98866655-98866656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552417771	chr4:98866658-98866659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192545794	chr4:98866666-98866667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182365552	chr4:98866694-98866695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112099472	chr4:98866705-98866706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550346350	chr4:98866741-98866742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115709165	chr4:98866752-98866753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535886593	chr4:98866767-98866768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553861243	chr4:98866809-98866810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566039769	chr4:98866851-98866852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188056496	chr4:98866862-98866863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192681005	chr4:98866867-98866868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201591988	chr4:98866869-98866870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201952773	chr4:98866870-98866871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543603797	chr4:98866877-98866878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552361455	chr4:98866880-98866881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200542134	chr4:98866884-98866885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6819047	chr4:98866902-98866903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs573304650	chr4:98866920-98866921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574179057	chr4:98866937-98866938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541837407	chr4:98866974-98866975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145712265	chr4:98866982-98866983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527245953	chr4:98867007-98867008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77143449	chr4:98867039-98867040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564371609	chr4:98867052-98867053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531577057	chr4:98867060-98867061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185022790	chr4:98867085-98867086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568598582	chr4:98867151-98867152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529393781	chr4:98867186-98867187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74577386	chr4:98867233-98867234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557625327	chr4:98867246-98867247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189913295	chr4:98867247-98867248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539771911	chr4:98867268-98867269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191985231	chr4:98867269-98867270	Weak transcription	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98864400-98874800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:98873200-98873600	Enhancers	Dnd41	blood
3	chr4:98873600-98874400	Flanking Active TSS	Dnd41	blood
4	chr4:98874400-98875600	Enhancers	Dnd41	blood
5	chr4:98874800-98875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:98877800-98878200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:98882800-98884600	Weak transcription	Pancreas	Pancrea
8	chr4:98883000-98884000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr4:98884000-98886000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:98884600-98884800	ZNF genes & repeats	Pancreas	Pancrea
11	chr4:98885200-98885600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:98886000-98886600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
13	chr4:98886400-98886800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:98890200-98890600	ZNF genes & repeats	Brain Anterior Caudate	brain
15	chr4:98894800-98895200	ZNF genes & repeats	Pancreas	Pancrea
16	chr4:98895000-98895200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:98895200-98895600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:98907600-98907800	Enhancers	Fetal Kidney	kidney
19	chr4:98908000-98908400	Enhancers	Brain Angular Gyrus	brain
20	chr4:98908000-98908400	Enhancers	Dnd41	blood
21	chr4:98909000-98909400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr4:98915800-98916800	Enhancers	HMEC	breast
23	chr4:98916000-98916600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:98916000-98916800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:98916800-98918400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:98922400-98923000	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr4:98927400-98927600	Weak transcription	Gastric	stomach
28	chr4:98927800-98928000	ZNF genes & repeats	Gastric	stomach
29	chr4:98932200-98932400	ZNF genes & repeats	Pancreas	Pancrea
30	chr4:98932400-98938000	Weak transcription	Pancreas	Pancrea
31	chr4:98938000-98938200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:98938000-98938600	ZNF genes & repeats	Pancreas	Pancrea
33	chr4:98938000-98938800	ZNF genes & repeats	Adipose Nuclei	Adipose
34	chr4:98946800-98947000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:98947000-98948800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:98948400-98949600	Enhancers	Fetal Brain Male	brain
37	chr4:98948800-98949600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr4:98967400-98968600	Enhancers	HSMMtube	muscle
39	chr4:98968000-98968400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:98968000-98968600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:98968000-98968600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:98968200-98968400	ZNF genes & repeats	Pancreas	Pancrea
43	chr4:98968200-98968600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:98968400-98972000	Weak transcription	Pancreas	Pancrea
45	chr4:98982400-98982800	Enhancers	Dnd41	blood
46	chr4:98998600-99000000	Enhancers	Dnd41	blood
47	chr4:99014600-99015800	Enhancers	HMEC	breast
48	chr4:99014600-99016000	Enhancers	Fetal Intestine Large	intestine
49	chr4:99014600-99016000	Enhancers	Fetal Intestine Small	intestine
50	chr4:99014800-99015800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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