Variant report

Variant	esv1849959
Chromosome Location	chr4:70224638-70439322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1179)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70410642-70411138	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70361428-70361936	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70383793-70384506	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70296492-70296914	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70324166-70324568	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70296492-70296919	K562	blood:	n/a	n/a
8	ARID3A	chr4:70350802-70351141	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:70359216-70359556	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
11	ATF1	chr4:70296489-70296914	K562	blood:	n/a	n/a
12	ATF2	chr4:70333524-70333998	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr4:70296499-70296777	HepG2	liver:	n/a	n/a
14	ATF3	chr4:70296574-70296796	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr4:70296552-70296826	A549	lung:	n/a	n/a
16	ATF3	chr4:70296558-70296973	A549	lung:	n/a	n/a
17	BACH1	chr4:70296489-70296908	K562	blood:	n/a	n/a
18	BATF	chr4:70296589-70296863	GM12878	blood:	n/a	chr4:70296823-70296832
19	BATF	chr4:70367562-70367758	GM12878	blood:	n/a	chr4:70367695-70367706
20	BATF	chr4:70296590-70296824	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:70296551-70296867	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:70296569-70296786	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr4:70296596-70296779	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:70296603-70296770	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr4:70296548-70296829	A549	lung:	n/a	n/a
26	BCL3	chr4:70296436-70296843	A549	lung:	n/a	n/a
27	BCLAF1	chr4:70296549-70296826	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:70296485-70296909	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:70361410-70361902	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:70411954-70412152	K562	blood:	n/a	n/a
31	BHLHE40	chr4:70296483-70296924	K562	blood:	n/a	n/a
32	BRCA1	chr4:70296484-70296924	GM12878	blood:	n/a	n/a
33	BRCA1	chr4:70296486-70296910	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr4:70296483-70296909	HepG2	liver:	n/a	n/a
35	CBX3	chr4:70290507-70290706	K562	blood:	n/a	n/a
36	CCNT2	chr4:70296445-70296895	K562	blood:	n/a	n/a
37	CEBPB	chr4:70391715-70391830	H1-hESC	embryonic stem cell:	n/a	chr4:70391769-70391780
38	CEBPB	chr4:70296492-70296908	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:70319378-70319596	HepG2	liver:	n/a	chr4:70319545-70319556
40	CEBPB	chr4:70296486-70296925	K562	blood:	n/a	n/a
41	CEBPB	chr4:70324164-70324515	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:70383870-70384874	HepG2	liver:	n/a	chr4:70384445-70384456 chr4:70384443-70384454 chr4:70384757-70384769
43	CEBPB	chr4:70324294-70324494	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:70359098-70359325	K562	blood:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
45	CEBPB	chr4:70361482-70361691	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:70347375-70347559	A549	lung:	n/a	n/a
47	CEBPB	chr4:70339506-70339743	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
49	CEBPB	chr4:70296570-70296806	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:70359060-70359353	A549	lung:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70346347-70346397	SK-N-SH_RA	brain:	n/a
2	chr4:70346347-70346397	PFSK-1	brain:	n/a
3	chr4:70346347-70346397	SAEC	small airway:	n/a
4	chr4:70389517-70389567	AG04449	skin:	fetal
5	chr4:70361062-70361112	HMEC	breast:	n/a
6	chr4:70389517-70389567	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:70346347-70346397	MCF-7	breast:	n/a
8	chr4:70361062-70361112	HRE	kidney:	n/a
9	chr4:70389517-70389567	HAEpiC	amniotic membrane:	n/a
10	chr4:70346347-70346397	NHDF-neo	bronchial:	n/a
11	chr4:70389517-70389567	GM12891	blood:	n/a
12	chr4:70361062-70361112	AG09309	skin:	n/a
13	chr4:70389517-70389567	IMR90	lung:	fetal
14	chr4:70346347-70346397	AG10803	skin:	n/a
15	chr4:70389517-70389567	HCM	heart:	n/a
16	chr4:70346347-70346397	NH-A	brain:	n/a
17	chr4:70346347-70346397	PANC-1	pancreas:	n/a
18	chr4:70389517-70389567	HRCEpiC	kidney:	n/a
19	chr4:70346347-70346397	NT2-D1	testis:	n/a
20	chr4:70346347-70346397	AoSMC	blood vessel:	n/a
21	chr4:70389517-70389567	Hela-S3	cervix:	n/a
22	chr4:70361062-70361112	K562	blood:	n/a
23	chr4:70361062-70361112	A549	lung:	n/a
24	chr4:70361062-70361112	HCF	heart:	n/a
25	chr4:70346347-70346397	IMR90	lung:	fetal
26	chr4:70346347-70346397	GM12878	blood:	n/a
27	chr4:70346347-70346397	CMK	blood:	n/a
28	chr4:70389517-70389567	BE2_C	brain:	n/a
29	chr4:70389517-70389567	AoSMC	blood vessel:	n/a
30	chr4:70361062-70361112	AG04450	lung:	fetal
31	chr4:70346347-70346397	HUVEC	blood vessel:	n/a
32	chr4:70346347-70346397	AG04449	skin:	fetal
33	chr4:70361062-70361112	HUVEC	blood vessel:	n/a
34	chr4:70389517-70389567	HIPEpiC	eye:	n/a
35	chr4:70361062-70361112	GM12891	blood:	n/a
36	chr4:70346347-70346397	Hela-S3	cervix:	n/a
37	chr4:70361062-70361112	SK-N-MC	brain:	n/a
38	chr4:70361062-70361112	GM12892	blood:	n/a
39	chr4:70389517-70389567	HepG2	liver:	n/a
40	chr4:70361062-70361112	RPTEC	kidney:	n/a
41	chr4:70361062-70361112	PFSK-1	brain:	n/a
42	chr4:70361062-70361112	PANC-1	pancreas:	n/a
43	chr4:70361062-70361112	HAEpiC	amniotic membrane:	n/a
44	chr4:70346347-70346397	SK-N-SH	brain:	n/a
45	chr4:70389517-70389567	SK-N-MC	brain:	n/a
46	chr4:70346347-70346397	ovcar-3	ovarian:	n/a
47	chr4:70346347-70346397	HEEpiC	esophagus:	n/a
48	chr4:70361062-70361112	GM12878	blood:	n/a
49	chr4:70346347-70346397	AG04450	lung:	fetal
50	chr4:70346347-70346397	GM06990	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
2	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:
3	chr4:70411496..70413587-chr4:70423922..70425853,2	K562	blood:
4	chr19:24184130..24184632-chr4:70296678..70297183,2	MCF-7	breast:
5	chr19:24183615..24184637-chr4:70296138..70296644,3	K562	blood:
6	chr4:70379330..70381215-chr4:70382030..70384687,2	K562	blood:
7	chr21:9825015..9827465-chr4:70296669..70298179,2	K562	blood:
8	chr4:70411496..70413587-chr4:70423922..70425853,2	K562	blood:
9	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
10	chr19:36066562..36067220-chr4:70296617..70297159,2	MCF-7	breast:
11	chr12:6797888..6800431-chr4:70351986..70354075,2	MCF-7	breast:
12	chr21:9824058..9826515-chr4:70295211..70298169,2	K562	blood:
13	chr2:133038471..133039156-chr4:70296229..70297178,3	MCF-7	breast:
14	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
15	chr2:169797130..169797902-chr4:70311918..70312713,2	MCF-7	breast:
16	chr4:70383119..70384022-chr4:70482515..70483454,3	MCF-7	breast:
17	chr20:52578439..52580096-chr4:70380828..70382348,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763
2	lnc-UGT2B28-7	chr4:70317229-70317331	NONHSAT096766
3	lnc-UGT2B28-6	chr4:70303075-70303156	NONHSAT096765
4	lnc-UGT2B28-6	chr4:70306600-70306768	NONHSAT096765
5	lnc-UGT2B28-7	chr4:70315732-70315864	NONHSAT096766
6	lnc-UGT2B28-6	chr4:70304044-70304260	NONHSAT096765
7	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764

No data

Variant related genes	Relation type
ENSG00000248824	TF binding region
UGT2A3P7	TF binding region
ENSG00000249686	TF binding region
ENSG00000268209	TF binding region
ENSG00000215110	TF binding region
ENSG00000264696	TF binding region
ENSG00000250828	TF binding region
ENSG00000249956	TF binding region
UGT2B4	TF binding region
ENSG00000248824	CpG island
UGT2A3P7	CpG island
ENSG00000249686	CpG island
ENSG00000268209	CpG island
ENSG00000215110	CpG island
ENSG00000264696	CpG island
ENSG00000250828	CpG island
ENSG00000249956	CpG island
UGT2B4	CpG island
ENSG00000264063	chromatin interactions
ENSG00000248886	chromatin interactions
ENSG00000126746	chromatin interactions
ENSG00000264462	chromatin interactions

Extended variants
information (count: 4625 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4625 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539766468	chr4:70224654-70224655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186885168	chr4:70224679-70224680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573133120	chr4:70224766-70224767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535544601	chr4:70224780-70224781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555485607	chr4:70224794-70224795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190831239	chr4:70224810-70224811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13127365	chr4:70224891-70224892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544552099	chr4:70224897-70224898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372526647	chr4:70224930-70224931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183344642	chr4:70224963-70224964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4345243	chr4:70224966-70224967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540196223	chr4:70225028-70225029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs118068311	chr4:70225029-70225030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529150736	chr4:70225039-70225040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200158423	chr4:70225136-70225137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13117652	chr4:70225140-70225141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs540560600	chr4:70225143-70225144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560392191	chr4:70225150-70225151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532613902	chr4:70225154-70225155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562530705	chr4:70225155-70225156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531323742	chr4:70225248-70225249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552488797	chr4:70225274-70225275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551329607	chr4:70225278-70225279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374991190	chr4:70225453-70225454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13118473	chr4:70225464-70225465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs576313394	chr4:70225472-70225473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533661673	chr4:70225490-70225491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530525473	chr4:70225505-70225506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546929185	chr4:70225516-70225517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186314238	chr4:70225615-70225616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535603686	chr4:70225626-70225627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555549263	chr4:70225637-70225638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191037190	chr4:70225652-70225653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567284148	chr4:70225658-70225659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116821120	chr4:70225668-70225669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558118984	chr4:70225697-70225698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371333064	chr4:70225732-70225733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540520256	chr4:70225833-70225834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554064341	chr4:70225910-70225911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536236263	chr4:70225913-70225914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182691436	chr4:70225935-70225936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542810769	chr4:70225938-70225939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561861097	chr4:70225943-70225944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546942021	chr4:70225956-70225957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562695545	chr4:70226044-70226045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531413412	chr4:70226061-70226062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544809890	chr4:70226078-70226079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564886926	chr4:70226080-70226081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527341869	chr4:70226081-70226082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546990624	chr4:70226085-70226086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70221200-70226200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:70225400-70226400	Enhancers	Fetal Intestine Large	intestine
3	chr4:70225400-70226800	Enhancers	Fetal Intestine Small	intestine
4	chr4:70226000-70226400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr4:70226200-70226400	Active TSS	Duodenum Mucosa	Duodenum
6	chr4:70226200-70226600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:70226400-70226600	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr4:70226600-70228000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:70228000-70228400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:70244200-70244800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr4:70265000-70265400	Enhancers	Fetal Heart	heart
12	chr4:70295800-70296400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr4:70296400-70296800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:70296400-70297000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr4:70296400-70297000	ZNF genes & repeats	Gastric	stomach
16	chr4:70296400-70297000	ZNF genes & repeats	Right Atrium	heart
17	chr4:70296400-70297000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
18	chr4:70296400-70297000	Flanking Bivalent TSS/Enh	Spleen	Spleen
19	chr4:70296600-70296800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:70296600-70296800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
23	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:70296600-70296800	ZNF genes & repeats	Primary B cells from cord blood	blood
25	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
26	chr4:70296600-70296800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr4:70296600-70296800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
29	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
30	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
31	chr4:70296600-70296800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
32	chr4:70296600-70296800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
33	chr4:70296600-70296800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:70296600-70296800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:70296600-70296800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
39	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Aorta	Aorta
40	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
41	chr4:70296600-70296800	ZNF genes & repeats	Brain Germinal Matrix	brain
42	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
43	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
44	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
45	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
46	chr4:70296600-70296800	Bivalent Enhancer	Fetal Heart	heart
47	chr4:70296600-70296800	ZNF genes & repeats	Fetal Kidney	kidney
48	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
49	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Placenta	Placenta
50	chr4:70296600-70296800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach

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