Variant report

Variant	nsv829927
Chromosome Location	chr4:49160366-49246621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2293)
CpG islands
(count:549)
Chromatin interactive
region (count:0)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2293 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:49219672-49219782	K562	blood:	n/a	n/a
2	ATF1	chr4:49168855-49169084	K562	blood:	n/a	n/a
3	ATF1	chr4:49163055-49163411	K562	blood:	n/a	n/a
4	ATF3	chr4:49163110-49163368	K562	blood:	n/a	chr4:49163223-49163236
5	BATF	chr4:49203975-49204281	GM12878	blood:	n/a	n/a
6	BATF	chr4:49167021-49167630	GM12878	blood:	n/a	n/a
7	BATF	chr4:49164575-49165145	GM12878	blood:	n/a	n/a
8	BATF	chr4:49182780-49183741	GM12878	blood:	n/a	n/a
9	BATF	chr4:49183830-49184242	GM12878	blood:	n/a	n/a
10	BATF	chr4:49165753-49166030	GM12878	blood:	n/a	n/a
11	BATF	chr4:49196524-49196831	GM12878	blood:	n/a	n/a
12	BATF	chr4:49199682-49200057	GM12878	blood:	n/a	n/a
13	BATF	chr4:49182870-49183109	GM12878	blood:	n/a	n/a
14	BATF	chr4:49186720-49187236	GM12878	blood:	n/a	n/a
15	BATF	chr4:49166572-49166917	GM12878	blood:	n/a	n/a
16	BATF	chr4:49193638-49193955	GM12878	blood:	n/a	n/a
17	BATF	chr4:49193971-49194254	GM12878	blood:	n/a	n/a
18	BATF	chr4:49196588-49196834	GM12878	blood:	n/a	n/a
19	BATF	chr4:49211509-49211776	GM12878	blood:	n/a	n/a
20	BATF	chr4:49181930-49182132	GM12878	blood:	n/a	n/a
21	BATF	chr4:49200625-49200836	GM12878	blood:	n/a	n/a
22	BATF	chr4:49194228-49194538	GM12878	blood:	n/a	n/a
23	BATF	chr4:49180996-49181347	GM12878	blood:	n/a	n/a
24	BATF	chr4:49187844-49188518	GM12878	blood:	n/a	n/a
25	BATF	chr4:49201857-49202145	GM12878	blood:	n/a	n/a
26	BATF	chr4:49168233-49168605	GM12878	blood:	n/a	n/a
27	BATF	chr4:49197009-49197431	GM12878	blood:	n/a	n/a
28	BATF	chr4:49161475-49161773	GM12878	blood:	n/a	n/a
29	BATF	chr4:49163630-49163944	GM12878	blood:	n/a	n/a
30	BATF	chr4:49165350-49165585	GM12878	blood:	n/a	n/a
31	BATF	chr4:49198280-49198474	GM12878	blood:	n/a	n/a
32	BATF	chr4:49226213-49226403	GM12878	blood:	n/a	n/a
33	BATF	chr4:49203258-49203635	GM12878	blood:	n/a	n/a
34	BATF	chr4:49186781-49187365	GM12878	blood:	n/a	n/a
35	BATF	chr4:49200088-49200392	GM12878	blood:	n/a	n/a
36	BATF	chr4:49191276-49191577	GM12878	blood:	n/a	n/a
37	BATF	chr4:49196142-49196389	GM12878	blood:	n/a	n/a
38	BATF	chr4:49200948-49201240	GM12878	blood:	n/a	n/a
39	BATF	chr4:49178953-49179255	GM12878	blood:	n/a	n/a
40	BATF	chr4:49187369-49187639	GM12878	blood:	n/a	n/a
41	BATF	chr4:49240544-49240716	GM12878	blood:	n/a	n/a
42	BATF	chr4:49185256-49185588	GM12878	blood:	n/a	n/a
43	BATF	chr4:49203192-49203619	GM12878	blood:	n/a	n/a
44	BATF	chr4:49196148-49196381	GM12878	blood:	n/a	n/a
45	BATF	chr4:49187322-49187755	GM12878	blood:	n/a	n/a
46	BATF	chr4:49163710-49164159	GM12878	blood:	n/a	n/a
47	BATF	chr4:49181450-49181651	GM12878	blood:	n/a	n/a
48	BATF	chr4:49166945-49167645	GM12878	blood:	n/a	n/a
49	BATF	chr4:49200976-49201419	GM12878	blood:	n/a	n/a
50	BATF	chr4:49168400-49168826	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:49163755-49163805	BE2_C	brain:	n/a
2	chr4:49163558-49163608	U87	brain:	n/a
3	chr4:49237109-49237159	ECC-1	luminal epithelium:	n/a
4	chr4:49236405-49236455	HAEpiC	amniotic membrane:	n/a
5	chr4:49164979-49165029	GM19239	blood:	n/a
6	chr4:49237497-49237547	AG09319	gingival:	n/a
7	chr4:49166489-49166539	HNPCEpiC	eye:	n/a
8	chr4:49163558-49163608	HIPEpiC	eye:	n/a
9	chr4:49237497-49237547	GM12892	blood:	n/a
10	chr4:49237109-49237159	SK-N-SH_RA	brain:	n/a
11	chr4:49237497-49237547	AG10803	skin:	n/a
12	chr4:49164979-49165029	Hepatocyte	liver:	n/a
13	chr4:49163755-49163805	ECC-1	luminal epithelium:	n/a
14	chr4:49204696-49204746	HUVEC	blood vessel:	n/a
15	chr4:49166489-49166539	AoSMC	blood vessel:	n/a
16	chr4:49237109-49237159	Hepatocyte	liver:	n/a
17	chr4:49164979-49165029	GM12878	blood:	n/a
18	chr4:49236405-49236455	ovcar-3	ovarian:	n/a
19	chr4:49204696-49204746	HMEC	breast:	n/a
20	chr4:49237109-49237159	HCM	heart:	n/a
21	chr4:49163276-49163326	U87	brain:	n/a
22	chr4:49236405-49236455	HEK293	kidney:	embryo
23	chr4:49164979-49165029	GM12892	blood:	n/a
24	chr4:49163276-49163326	MCF-7	breast:	n/a
25	chr4:49237497-49237547	A549	lung:	n/a
26	chr4:49236405-49236455	SAEC	small airway:	n/a
27	chr4:49163276-49163326	CMK	blood:	n/a
28	chr4:49163558-49163608	ECC-1	luminal epithelium:	n/a
29	chr4:49166489-49166539	RPTEC	kidney:	n/a
30	chr4:49237497-49237547	HAEpiC	amniotic membrane:	n/a
31	chr4:49163755-49163805	HMEC	breast:	n/a
32	chr4:49236405-49236455	SK-N-SH	brain:	n/a
33	chr4:49163755-49163805	GM06990	blood:	n/a
34	chr4:49236405-49236455	ProgFib	skin:	n/a
35	chr4:49163276-49163326	SAEC	small airway:	n/a
36	chr4:49166489-49166539	HRE	kidney:	n/a
37	chr4:49163558-49163608	IMR90	lung:	fetal
38	chr4:49237497-49237547	GM12878	blood:	n/a
39	chr4:49163755-49163805	Caco-2	colon:	n/a
40	chr4:49204696-49204746	SAEC	small airway:	n/a
41	chr4:49237497-49237547	HL-60	blood:	n/a
42	chr4:49163558-49163608	HCPEpiC	choroid plexus:	n/a
43	chr4:49163755-49163805	SK-N-SH_RA	brain:	n/a
44	chr4:49166489-49166539	U87	brain:	n/a
45	chr4:49204696-49204746	HCPEpiC	choroid plexus:	n/a
46	chr4:49237497-49237547	AG04450	lung:	fetal
47	chr4:49166489-49166539	ProgFib	skin:	n/a
48	chr4:49163276-49163326	HUVEC	blood vessel:	n/a
49	chr4:49166489-49166539	Jurkat	blood:	n/a
50	chr4:49236405-49236455	HMEC	breast:	n/a

No data

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCIAD2-5	chr4:49214268-49214641	NONHSAT096314
2	lnc-OCIAD2-9	chr4:49246290-49246387	NONHSAT096322
3	lnc-OCIAD2-9	chr4:49239116-49239167	NONHSAT096322
4	lnc-CWH43-2	chr4:49175125-49175286	NONHSAT096308
5	lnc-OCIAD2-6	chr4:49221527-49221803	NONHSAT096315
6	lnc-CWH43-2	chr4:49171338-49171778	NONHSAT096308
7	lnc-OCIAD2-9	chr4:49241263-49241308	NONHSAT096322
8	lnc-OCIAD2-9	chr4:49240040-49240093	NONHSAT096322
9	lnc-OCIAD2-9	chr4:49239669-49239711	NONHSAT096322
10	lnc-OCIAD2-9	chr4:49244726-49244948	NONHSAT096322
11	lnc-OCIAD2-7	chr4:49231590-49233301	NONHSAT096320

No data

Variant related genes	Relation type
ENSG00000249079	TF binding region
ENSG00000249828	TF binding region
ENSG00000222437	TF binding region
ENSG00000237961	TF binding region
ENSG00000268736	TF binding region
SNX18P23	TF binding region
ENSG00000221415	TF binding region
ENSG00000221747	TF binding region
ENSG00000266337	TF binding region
ENSG00000248946	TF binding region
ENSG00000249079	CpG island
ENSG00000249828	CpG island
ENSG00000222437	CpG island
ENSG00000237961	CpG island
ENSG00000268736	CpG island
SNX18P23	CpG island
ENSG00000221415	CpG island
ENSG00000221747	CpG island
ENSG00000266337	CpG island
ENSG00000248946	CpG island

Extended variants
information (count: 5484 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5484 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145671295	chr4:49160376-49160377	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78246318	chr4:49160383-49160384	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184455431	chr4:49160404-49160405	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77702137	chr4:49160406-49160407	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10938555	chr4:49160407-49160408	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75909530	chr4:49160412-49160413	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76685401	chr4:49160419-49160420	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9985572	chr4:49160424-49160425	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75848196	chr4:49160439-49160440	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147984514	chr4:49160452-49160453	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77254108	chr4:49160453-49160454	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75278117	chr4:49160457-49160458	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80284418	chr4:49160458-49160459	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199738643	chr4:49160461-49160462	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78746598	chr4:49160464-49160465	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143319603	chr4:49160465-49160466	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78043793	chr4:49160466-49160467	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200768031	chr4:49160467-49160468	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147844687	chr4:49160469-49160470	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139181331	chr4:49160488-49160489	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78880950	chr4:49160489-49160490	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563389588	chr4:49160502-49160503	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202042061	chr4:49160508-49160509	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79488392	chr4:49160510-49160511	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7664998	chr4:49160511-49160512	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74801767	chr4:49160512-49160513	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79087320	chr4:49160517-49160518	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201564293	chr4:49160530-49160531	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7665157	chr4:49160534-49160535	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78194874	chr4:49160539-49160540	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377386552	chr4:49160541-49160542	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146800949	chr4:49160543-49160544	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575583038	chr4:49160544-49160545	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7689100	chr4:49160548-49160549	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7665162	chr4:49160549-49160550	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs438024	chr4:49160559-49160560	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145912728	chr4:49160560-49160561	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370760197	chr4:49160561-49160562	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79617656	chr4:49160574-49160575	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376314323	chr4:49160578-49160579	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368521171	chr4:49160579-49160580	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10018356	chr4:49160593-49160594	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150246513	chr4:49160597-49160598	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75338412	chr4:49160598-49160599	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59874649	chr4:49160605-49160606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7665199	chr4:49160609-49160610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9985573	chr4:49160610-49160611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561212653	chr4:49160615-49160616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78768897	chr4:49160620-49160621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80234888	chr4:49160621-49160622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:49143000-49160600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr4:49158600-49163000	Weak transcription	K562	blood
3	chr4:49158600-49163400	Weak transcription	A549	lung
4	chr4:49158600-49163400	Weak transcription	NH-A	brain
5	chr4:49162000-49162200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:49162800-49163800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:49163000-49163800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:49163000-49163800	ZNF genes & repeats	Fetal Stomach	stomach
9	chr4:49163000-49163800	ZNF genes & repeats	Lung	lung
10	chr4:49163000-49164000	Active TSS	K562	blood
11	chr4:49163000-49166200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:49163200-49163600	ZNF genes & repeats	Thymus	Thymus
13	chr4:49163200-49163800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:49163200-49163800	ZNF genes & repeats	Left Ventricle	heart
15	chr4:49163200-49163800	ZNF genes & repeats	Pancreas	Pancrea
16	chr4:49163200-49164200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
17	chr4:49163400-49163800	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr4:49163400-49163800	ZNF genes & repeats	Esophagus	oesophagus
19	chr4:49163400-49163800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
20	chr4:49163400-49163800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
21	chr4:49163400-49163800	ZNF genes & repeats	Gastric	stomach
22	chr4:49163400-49163800	ZNF genes & repeats	A549	lung
23	chr4:49163400-49163800	ZNF genes & repeats	NH-A	brain
24	chr4:49163400-49163800	ZNF genes & repeats	NHDF-Ad	bronchial
25	chr4:49163400-49170600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:49163800-49170400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr4:49164000-49164400	Flanking Active TSS	K562	blood
28	chr4:49164400-49164600	Active TSS	K562	blood
29	chr4:49164600-49164800	Flanking Active TSS	K562	blood
30	chr4:49164800-49165800	Weak transcription	K562	blood
31	chr4:49165800-49166000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr4:49165800-49166200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:49165800-49166200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:49165800-49167400	Enhancers	K562	blood
35	chr4:49167400-49168200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr4:49167400-49168400	Weak transcription	K562	blood
37	chr4:49168000-49170400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr4:49168200-49169000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:49168200-49169200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
40	chr4:49168400-49169000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:49168400-49169200	Enhancers	K562	blood
42	chr4:49168400-49171400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr4:49168600-49169200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr4:49168600-49169200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
45	chr4:49168600-49169200	ZNF genes & repeats	Fetal Heart	heart
46	chr4:49168800-49169000	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
47	chr4:49168800-49169200	ZNF genes & repeats	Pancreas	Pancrea
48	chr4:49168800-49169200	Active TSS	Stomach Mucosa	stomach
49	chr4:49177000-49177400	Enhancers	K562	blood
50	chr4:49177000-49177800	ZNF genes & repeats	Adipose Nuclei	Adipose

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