Variant report

Variant	nsv595387
Chromosome Location	chr4:128410916-128523964
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	chr4:128460128-128460277	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:128438475-128438545	K562	blood:	n/a	n/a
3	ARID3A	chr4:128460020-128460281	K562	blood:	n/a	n/a
4	ARID3A	chr4:128426459-128426608	K562	blood:	n/a	n/a
5	ARID3A	chr4:128508162-128508384	K562	blood:	n/a	n/a
6	ARID3A	chr4:128522219-128522497	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:128454597-128454833	K562	blood:	n/a	n/a
8	ARID3A	chr4:128446821-128447141	K562	blood:	n/a	n/a
9	ATF1	chr4:128454392-128454859	K562	blood:	n/a	n/a
10	ATF1	chr4:128446814-128447100	K562	blood:	n/a	n/a
11	ATF1	chr4:128422271-128422576	K562	blood:	n/a	n/a
12	BHLHE40	chr4:128454410-128454963	K562	blood:	n/a	n/a
13	BHLHE40	chr4:128460072-128460251	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:128436599-128436691	K562	blood:	n/a	n/a
15	BHLHE40	chr4:128446814-128446968	K562	blood:	n/a	n/a
16	BRCA1	chr4:128460025-128460358	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr4:128436438-128436818	K562	blood:	n/a	n/a
18	CBX3	chr4:128451304-128451648	K562	blood:	n/a	n/a
19	CBX3	chr4:128454556-128454882	K562	blood:	n/a	n/a
20	CCNT2	chr4:128454291-128454871	K562	blood:	n/a	chr4:128454772-128454792
21	CCNT2	chr4:128426346-128426656	K562	blood:	n/a	n/a
22	CEBPB	chr4:128412781-128413072	K562	blood:	n/a	chr4:128412940-128412951 chr4:128412922-128412933
23	CEBPB	chr4:128522202-128522528	A549	lung:	n/a	chr4:128522333-128522344
24	CEBPB	chr4:128454578-128454866	K562	blood:	n/a	chr4:128454630-128454643
25	CEBPB	chr4:128445581-128445854	K562	blood:	n/a	n/a
26	CEBPB	chr4:128522158-128522515	K562	blood:	n/a	chr4:128522333-128522344
27	CEBPB	chr4:128507890-128508128	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:128434631-128434836	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:128522174-128522525	Hela-S3	cervix:	n/a	chr4:128522333-128522344
30	CEBPB	chr4:128519868-128520246	HepG2	liver:	n/a	chr4:128520051-128520060 chr4:128520051-128520062 chr4:128520049-128520060 chr4:128520051-128520060 chr4:128520051-128520060 chr4:128520051-128520060
31	CEBPB	chr4:128522147-128522464	A549	lung:	n/a	chr4:128522333-128522344
32	CEBPB	chr4:128522205-128522530	MCF-7	breast:	n/a	chr4:128522333-128522344
33	CEBPB	chr4:128519887-128520213	IMR90	lung:	n/a	chr4:128520051-128520060 chr4:128520051-128520062 chr4:128520049-128520060 chr4:128520051-128520060 chr4:128520051-128520060 chr4:128520051-128520060
34	CEBPB	chr4:128487097-128487297	HepG2	liver:	n/a	chr4:128487206-128487217
35	CEBPB	chr4:128412903-128413083	H1-hESC	embryonic stem cell:	n/a	chr4:128412940-128412951 chr4:128412922-128412933
36	CEBPB	chr4:128479181-128479305	K562	blood:	n/a	chr4:128479194-128479205
37	CEBPB	chr4:128479070-128479295	HepG2	liver:	n/a	chr4:128479194-128479205
38	CEBPB	chr4:128421118-128421321	HepG2	liver:	n/a	chr4:128421178-128421189
39	CEBPB	chr4:128508025-128508188	A549	lung:	n/a	n/a
40	CEBPB	chr4:128519881-128520223	K562	blood:	n/a	chr4:128520051-128520060 chr4:128520051-128520062 chr4:128520049-128520060 chr4:128520051-128520060 chr4:128520051-128520060 chr4:128520051-128520060
41	CEBPB	chr4:128425773-128426012	K562	blood:	n/a	n/a
42	CEBPB	chr4:128487089-128487289	IMR90	lung:	n/a	chr4:128487206-128487217
43	CEBPB	chr4:128519896-128520180	A549	lung:	n/a	chr4:128520051-128520060 chr4:128520051-128520062 chr4:128520049-128520060 chr4:128520051-128520060 chr4:128520051-128520060 chr4:128520051-128520060
44	CEBPB	chr4:128521996-128522656	HCT-116	colon:	n/a	chr4:128522333-128522344
45	CEBPB	chr4:128522188-128522465	MCF-7	breast:	n/a	chr4:128522333-128522344
46	CEBPB	chr4:128445594-128445796	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:128522203-128522428	HepG2	liver:	n/a	chr4:128522333-128522344
48	CEBPB	chr4:128445643-128445788	A549	lung:	n/a	n/a
49	CEBPB	chr4:128444575-128444819	K562	blood:	n/a	n/a
50	CEBPB	chr4:128412785-128413068	HepG2	liver:	n/a	chr4:128412940-128412951 chr4:128412922-128412933

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128461763-128461813	GM12878	blood:	n/a
2	chr4:128440118-128440168	Hepatocyte	liver:	n/a
3	chr4:128461763-128461813	NT2-D1	testis:	n/a
4	chr4:128430108-128430158	BE2_C	brain:	n/a
5	chr4:128461763-128461813	HEK293	kidney:	embryo
6	chr4:128430108-128430158	LNCaP	prostate:	n/a
7	chr4:128440118-128440168	GM12892	blood:	n/a
8	chr4:128461763-128461813	HRE	kidney:	n/a
9	chr4:128430108-128430158	HNPCEpiC	eye:	n/a
10	chr4:128430108-128430158	SK-N-SH_RA	brain:	n/a
11	chr4:128461763-128461813	Hela-S3	cervix:	n/a
12	chr4:128430108-128430158	HIPEpiC	eye:	n/a
13	chr4:128461763-128461813	HCPEpiC	choroid plexus:	n/a
14	chr4:128430108-128430158	SKMC	muscle:	n/a
15	chr4:128440118-128440168	AoSMC	blood vessel:	n/a
16	chr4:128430108-128430158	Caco-2	colon:	n/a
17	chr4:128430108-128430158	PrEC	prostate:	n/a
18	chr4:128430108-128430158	NH-A	brain:	n/a
19	chr4:128430108-128430158	Hepatocyte	liver:	n/a
20	chr4:128461763-128461813	AG09309	skin:	n/a
21	chr4:128440118-128440168	ECC-1	luminal epithelium:	n/a
22	chr4:128440118-128440168	SAEC	small airway:	n/a
23	chr4:128440118-128440168	GM12891	blood:	n/a
24	chr4:128430108-128430158	HRPEpiC	eye:	n/a
25	chr4:128461763-128461813	PFSK-1	brain:	n/a
26	chr4:128461763-128461813	H1-hESC	embryonic stem cell:	embryo
27	chr4:128430108-128430158	AG10803	skin:	n/a
28	chr4:128461763-128461813	CMK	blood:	n/a
29	chr4:128440118-128440168	HEK293	kidney:	embryo
30	chr4:128440118-128440168	HRE	kidney:	n/a
31	chr4:128430108-128430158	GM12892	blood:	n/a
32	chr4:128430108-128430158	NT2-D1	testis:	n/a
33	chr4:128430108-128430158	AG04449	skin:	fetal
34	chr4:128461763-128461813	Jurkat	blood:	n/a
35	chr4:128430108-128430158	HAEpiC	amniotic membrane:	n/a
36	chr4:128440118-128440168	HUVEC	blood vessel:	n/a
37	chr4:128440118-128440168	CMK	blood:	n/a
38	chr4:128461763-128461813	GM12892	blood:	n/a
39	chr4:128430108-128430158	Hela-S3	cervix:	n/a
40	chr4:128430108-128430158	HMEC	breast:	n/a
41	chr4:128461763-128461813	K562	blood:	n/a
42	chr4:128440118-128440168	HIPEpiC	eye:	n/a
43	chr4:128461763-128461813	ovcar-3	ovarian:	n/a
44	chr4:128440118-128440168	HAEpiC	amniotic membrane:	n/a
45	chr4:128430108-128430158	HCM	heart:	n/a
46	chr4:128430108-128430158	SAEC	small airway:	n/a
47	chr4:128461763-128461813	AG09319	gingival:	n/a
48	chr4:128440118-128440168	A549	lung:	n/a
49	chr4:128440118-128440168	ProgFib	skin:	n/a
50	chr4:128440118-128440168	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:128459720..128460439-chr4:128507855..128508488,3	MCF-7	breast:
2	chr4:128486825..128490042-chr4:128490605..128492933,3	K562	blood:
3	chr4:128449129..128451520-chr4:128453107..128455386,2	K562	blood:
4	chr4:128438189..128441215-chr4:128442876..128446018,3	K562	blood:
5	chr4:128522468..128525015-chr4:128578213..128580607,2	K562	blood:
6	chr4:128517807..128520634-chr4:128521917..128524508,2	K562	blood:
7	chr4:128449705..128452234-chr4:128453227..128455144,2	K562	blood:
8	chr4:128521727..128523968-chr4:128577085..128579713,2	K562	blood:
9	chr4:128490719..128492998-chr4:128553129..128556082,2	K562	blood:
10	chr4:128522143..128525025-chr4:128539109..128540702,2	K562	blood:
11	chr4:128449129..128451520-chr4:128453107..128455386,2	K562	blood:
12	chr4:128449705..128452234-chr4:128453227..128455144,2	K562	blood:
13	chr3:119865708..119866577-chr4:128412232..128412732,2	MCF-7	breast:
14	chr4:128497413..128500074-chr4:128505896..128508169,2	MCF-7	breast:
15	chr4:128486825..128490042-chr4:128490605..128492933,3	K562	blood:
16	chr4:128438189..128441215-chr4:128442876..128446018,3	K562	blood:
17	chr4:128497413..128500074-chr4:128505896..128508169,2	MCF-7	breast:
18	chr4:128375252..128378171-chr4:128454899..128457356,2	K562	blood:
19	chr4:128517807..128520634-chr4:128521917..128524508,2	K562	blood:
20	chr4:128459720..128460439-chr4:128507855..128508488,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTU-1	chr4:128419482-128419962	NONHSAT098238
2	lnc-MFSD8-9	chr4:128492862-128492960	l_2728_chr4:128237735-128492960_lung
3	lnc-INTU-2	chr4:128414660-128414983	NONHSAT098237

Variant related genes	Relation type
ENSG00000248209	TF binding region
ENSG00000249795	TF binding region
ENSG00000248209	CpG island
ENSG00000249795	CpG island
ENSG00000164066	chromatin interactions

Extended variants
information (count: 2637 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2002543	chr4:128410916-128410917	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572529859	chr4:128410987-128410988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535168266	chr4:128410990-128410991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568947281	chr4:128411217-128411218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs115175334	chr4:128411506-128411507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs141482805	chr4:128412207-128412208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34587835	chr4:128412240-128412241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558248453	chr4:128412256-128412257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150869783	chr4:128412265-128412266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544397276	chr4:128412305-128412306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188498617	chr4:128412351-128412352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574663919	chr4:128412358-128412359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181309272	chr4:128412373-128412374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114977309	chr4:128412374-128412375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140095140	chr4:128412438-128412439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576624933	chr4:128412462-128412463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547080938	chr4:128412466-128412467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372566972	chr4:128412551-128412552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186596096	chr4:128412581-128412582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559528473	chr4:128412729-128412730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200847198	chr4:128412805-128412806	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs565387565	chr4:128412871-128412872	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs543308355	chr4:128412885-128412886	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs532700649	chr4:128412890-128412891	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs77218152	chr4:128412894-128412895	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs149198310	chr4:128412946-128412947	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201559846	chr4:128412948-128412949	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551146587	chr4:128412949-128412950	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs569386129	chr4:128412978-128412979	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377424613	chr4:128412993-128412994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs530398608	chr4:128413012-128413013	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs191961338	chr4:128413024-128413025	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs373245483	chr4:128413036-128413037	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs556879379	chr4:128413054-128413055	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566098586	chr4:128413197-128413198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533554170	chr4:128413201-128413202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181841882	chr4:128413235-128413236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537581129	chr4:128413245-128413246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556304818	chr4:128413248-128413249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34757568	chr4:128413333-128413334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187298478	chr4:128413358-128413359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191038134	chr4:128413369-128413370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144055157	chr4:128413398-128413399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182184870	chr4:128413410-128413411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540629306	chr4:128413449-128413450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565320417	chr4:128413500-128413501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532623892	chr4:128413522-128413523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147326552	chr4:128413548-128413549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35000151	chr4:128413559-128413560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397808964	chr4:128413566-128413567	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
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
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
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128409400-128411000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:128410600-128411000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:128412200-128413600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:128419200-128422400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:128419400-128419800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:128419800-128421600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:128419800-128422800	Enhancers	Fetal Heart	heart
8	chr4:128421600-128422000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:128421600-128422800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr4:128421600-128423000	Enhancers	Fetal Lung	lung
11	chr4:128421800-128422600	Enhancers	Ovary	ovary
12	chr4:128421800-128422800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:128421800-128422800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:128421800-128422800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:128421800-128422800	Enhancers	NH-A	brain
16	chr4:128421800-128424000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:128422000-128422200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:128422000-128422600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:128422000-128422600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:128422000-128422600	Enhancers	Fetal Muscle Leg	muscle
21	chr4:128422000-128422600	Enhancers	Left Ventricle	heart
22	chr4:128422000-128422600	Enhancers	Right Ventricle	heart
23	chr4:128422000-128422800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr4:128422000-128422800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:128422000-128422800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:128422000-128423000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:128422000-128423000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:128422000-128424800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:128422000-128424800	Enhancers	NHDF-Ad	bronchial
30	chr4:128422000-128426000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:128422200-128422600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:128422200-128422600	Enhancers	K562	blood
33	chr4:128422200-128422800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:128422200-128422800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:128422200-128423600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:128422400-128422800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:128422400-128422800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:128422400-128423000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:128422400-128423200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:128422600-128422800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr4:128422600-128426400	Weak transcription	Fetal Muscle Leg	muscle
42	chr4:128422600-128426400	Weak transcription	K562	blood
43	chr4:128422600-128427000	Weak transcription	Left Ventricle	heart
44	chr4:128422600-128427000	Weak transcription	Ovary	ovary
45	chr4:128422600-128427000	Weak transcription	Right Ventricle	heart
46	chr4:128422600-128427400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:128422800-128423200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr4:128422800-128423400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:128422800-128423800	Weak transcription	NH-A	brain
50	chr4:128422800-128424000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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