Variant report

Variant	nsv508308
Chromosome Location	chr4:122278897-122312719
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	chr4:122291909-122292227	K562	blood:	n/a	n/a
2	ATF3	chr4:122297220-122297606	HCT-116	colon:	n/a	n/a
3	BACH1	chr4:122302125-122302144	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr4:122301623-122301829	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr4:122297242-122297685	HCT-116	colon:	n/a	n/a
6	CBX3	chr4:122297146-122297654	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:122302243-122302593	IMR90	lung:	n/a	chr4:122302415-122302426
8	CEBPB	chr4:122308004-122308138	A549	lung:	n/a	chr4:122308041-122308052
9	CEBPB	chr4:122279636-122280024	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:122302248-122302553	K562	blood:	n/a	chr4:122302415-122302426
11	CEBPB	chr4:122296277-122296972	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:122279585-122280164	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:122296462-122296778	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:122302250-122302592	HepG2	liver:	n/a	chr4:122302415-122302426
15	CEBPB	chr4:122302332-122302494	ECC-1	luminal epithelium:	n/a	chr4:122302415-122302426
16	CEBPB	chr4:122279673-122279986	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:122296251-122296905	HCT-116	colon:	n/a	n/a
18	CEBPB	chr4:122302251-122302514	MCF-7	breast:	n/a	chr4:122302415-122302426
19	CEBPB	chr4:122279438-122280199	HCT-116	colon:	n/a	n/a
20	CEBPB	chr4:122302270-122302593	A549	lung:	n/a	chr4:122302415-122302426
21	CEBPB	chr4:122279663-122280040	A549	lung:	n/a	n/a
22	CEBPB	chr4:122288309-122288515	HepG2	liver:	n/a	chr4:122288383-122288394
23	CEBPB	chr4:122307924-122308124	IMR90	lung:	n/a	chr4:122308041-122308052
24	CEBPB	chr4:122302127-122302599	H1-hESC	embryonic stem cell:	n/a	chr4:122302415-122302426
25	CEBPB	chr4:122302361-122302482	Hela-S3	cervix:	n/a	chr4:122302415-122302426
26	CEBPB	chr4:122307883-122308189	HepG2	liver:	n/a	chr4:122308041-122308052
27	CHD1	chr4:122301712-122302022	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:122312514-122312705	K562	blood:	n/a	n/a
29	CHD2	chr4:122301636-122301827	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr4:122301420-122301840	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:122292100-122292250	HMEC	breast:	n/a	n/a
32	CTCF	chr4:122302240-122302390	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr4:122291980-122292130	NHDF-neo	bronchial:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
34	CTCF	chr4:122291980-122292130	GM12864	blood:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
35	CTCF	chr4:122292020-122292170	HCPEpiC	choroid plexus:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
36	CTCF	chr4:122291980-122292130	SAEC	small airway:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
37	CTCF	chr4:122291755-122292461	HCT-116	colon:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
38	CTCF	chr4:122298360-122298510	HMEC	breast:	n/a	n/a
39	CTCF	chr4:122291980-122292130	AG04450	lung:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
40	CTCF	chr4:122291986-122292129	A549	lung:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
41	CTCF	chr4:122291956-122292202	K562	blood:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
42	CTCF	chr4:122291960-122292110	GM12872	blood:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
43	CTCF	chr4:122291985-122292180	Kidney_OC	kidney:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
44	CTCF	chr4:122291960-122292110	GM12801	blood:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
45	CTCF	chr4:122291977-122292183	Pancreas_OC	pancreas:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
46	CTCF	chr4:122291696-122291780	A549	lung:	n/a	n/a
47	CTCF	chr4:122291710-122291816	GM12878	blood:	n/a	n/a
48	CTCF	chr4:122291980-122292130	HRE	kidney:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094
49	CTCF	chr4:122291640-122291790	GM12864	blood:	n/a	n/a
50	CTCF	chr4:122291592-122292410	A549	lung:	n/a	chr4:122292074-122292087 chr4:122292071-122292089 chr4:122292073-122292094

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122301996-122302046	GM12878	blood:	n/a
2	chr4:122302674-122302724	HEEpiC	esophagus:	n/a
3	chr4:122301996-122302046	GM12878	blood:	n/a
4	chr4:122302674-122302724	HEEpiC	esophagus:	n/a
5	chr4:122302674-122302724	LNCaP	prostate:	n/a
6	chr4:122302268-122302318	HIPEpiC	eye:	n/a
7	chr4:122301573-122301623	ovcar-3	ovarian:	n/a
8	chr4:122302680-122302730	A549	lung:	n/a
9	chr4:122302674-122302724	HCF	heart:	n/a
10	chr4:122302331-122302381	HEEpiC	esophagus:	n/a
11	chr4:122300140-122300190	HepG2	liver:	n/a
12	chr4:122305076-122305126	Caco-2	colon:	n/a
13	chr4:122302007-122302057	GM06990	blood:	n/a
14	chr4:122301740-122301790	HRE	kidney:	n/a
15	chr4:122302674-122302724	HRE	kidney:	n/a
16	chr4:122305076-122305126	Jurkat	blood:	n/a
17	chr4:122302265-122302315	HMEC	breast:	n/a
18	chr4:122301740-122301790	SKMC	muscle:	n/a
19	chr4:122301724-122301774	AoSMC	blood vessel:	n/a
20	chr4:122305076-122305126	PANC-1	pancreas:	n/a
21	chr4:122302232-122302282	HCPEpiC	choroid plexus:	n/a
22	chr4:122301740-122301790	LNCaP	prostate:	n/a
23	chr4:122301573-122301623	SK-N-MC	brain:	n/a
24	chr4:122300140-122300190	IMR90	lung:	fetal
25	chr4:122298456-122298506	PFSK-1	brain:	n/a
26	chr4:122302232-122302282	AG04449	skin:	fetal
27	chr4:122300140-122300190	HMEC	breast:	n/a
28	chr4:122302421-122302471	NH-A	brain:	n/a
29	chr4:122301816-122301866	ECC-1	luminal epithelium:	n/a
30	chr4:122301816-122301866	GM06990	blood:	n/a
31	chr4:122302268-122302318	AG04449	skin:	fetal
32	chr4:122301996-122302046	Caco-2	colon:	n/a
33	chr4:122302007-122302057	PFSK-1	brain:	n/a
34	chr4:122302674-122302724	HMEC	breast:	n/a
35	chr4:122301724-122301774	GM12878	blood:	n/a
36	chr4:122302268-122302318	HEK293	kidney:	embryo
37	chr4:122305076-122305126	SKMC	muscle:	n/a
38	chr4:122301724-122301774	HEEpiC	esophagus:	n/a
39	chr4:122302674-122302724	HIPEpiC	eye:	n/a
40	chr4:122302680-122302730	BE2_C	brain:	n/a
41	chr4:122302674-122302724	NHDF-neo	bronchial:	n/a
42	chr4:122305076-122305126	AG10803	skin:	n/a
43	chr4:122302007-122302057	BE2_C	brain:	n/a
44	chr4:122301816-122301866	AG09309	skin:	n/a
45	chr4:122302674-122302724	IMR90	lung:	fetal
46	chr4:122301816-122301866	NB4	blood:	n/a
47	chr4:122298456-122298506	AG09309	skin:	n/a
48	chr4:122300140-122300190	HL-60	blood:	n/a
49	chr4:122301573-122301623	U87	brain:	n/a
50	chr4:122301996-122302046	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:122265924..122266538-chr4:122292160..122292685,2	MCF-7	breast:
2	chr4:122305121..122307560-chr4:122314123..122316320,2	K562	blood:
3	chr4:122290131..122292541-chr4:122296588..122298243,2	K562	blood:
4	chr4:122291642..122292373-chr4:122577439..122577960,2	MCF-7	breast:
5	chr4:122291624..122292430-chr4:122342879..122343479,3	MCF-7	breast:
6	chr4:122198899..122199696-chr4:122292166..122292719,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNIP3-2	chr4:122290588-122291500	NONHSAT098140

Variant related genes	Relation type
QRFPR	TF binding region
ENSG00000213480	TF binding region
QRFPR	CpG island
ENSG00000213480	CpG island
ENSG00000213480	chromatin interactions

Extended variants
information (count: 1231 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528464550	chr4:122279070-122279071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145201070	chr4:122279071-122279072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182532533	chr4:122279134-122279135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528836858	chr4:122279142-122279143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185652729	chr4:122279171-122279172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72668974	chr4:122279192-122279193	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs56029221	chr4:122279269-122279270	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530067132	chr4:122279296-122279297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552524976	chr4:122279387-122279388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73845777	chr4:122279441-122279442	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553233513	chr4:122279543-122279544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35499324	chr4:122279575-122279576	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs535425510	chr4:122279656-122279657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538843479	chr4:122279678-122279679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555024571	chr4:122279723-122279724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575302580	chr4:122279766-122279767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190737357	chr4:122279769-122279770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558000126	chr4:122279824-122279825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11098615	chr4:122279840-122279841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577896547	chr4:122279900-122279901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540560510	chr4:122279908-122279909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111362008	chr4:122279933-122279934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115524667	chr4:122280011-122280012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4259086	chr4:122280041-122280042	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs570746941	chr4:122280070-122280071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12499042	chr4:122280132-122280133	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531450057	chr4:122280150-122280151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531054277	chr4:122280250-122280251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550624247	chr4:122280252-122280253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570742638	chr4:122280267-122280268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533348921	chr4:122280306-122280307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10518388	chr4:122280335-122280336	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs367575469	chr4:122280387-122280388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549946910	chr4:122280396-122280397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78932279	chr4:122280420-122280421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535730240	chr4:122280449-122280450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574491286	chr4:122280482-122280483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558587314	chr4:122280524-122280525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568727439	chr4:122280536-122280537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537974078	chr4:122280623-122280624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369340687	chr4:122280788-122280789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs70950808	chr4:122280789-122280790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34785724	chr4:122280800-122280801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6845337	chr4:122280802-122280803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7687450	chr4:122280804-122280805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540418915	chr4:122280806-122280807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553644358	chr4:122280808-122280809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6845821	chr4:122280810-122280811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368381339	chr4:122280813-122280814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6845341	chr4:122280814-122280815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122279000-122279400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:122279000-122280800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr4:122279200-122280400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:122279400-122279800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:122279400-122280200	Enhancers	NHEK	skin
6	chr4:122279400-122280400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:122279400-122280400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr4:122279400-122280600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:122279400-122280600	Enhancers	HMEC	breast
10	chr4:122279600-122280000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:122279600-122280400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:122279800-122280200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:122279800-122280400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:122279800-122280400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:122279800-122280400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:122280200-122281400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:122280200-122281600	Weak transcription	NHEK	skin
18	chr4:122280400-122280600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:122280400-122281400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:122280400-122281400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:122280400-122281600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:122280400-122281600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr4:122280600-122281000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:122280600-122281000	Weak transcription	HMEC	breast
25	chr4:122280600-122281200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:122280800-122281200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr4:122281000-122281200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:122281000-122282200	Enhancers	HMEC	breast
29	chr4:122281200-122282200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr4:122281200-122282200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr4:122281200-122283400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:122281400-122282200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:122281400-122282200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:122281600-122281800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:122281600-122282200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:122281600-122282200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr4:122281600-122282200	Enhancers	NHEK	skin
38	chr4:122282200-122294000	Weak transcription	HMEC	breast
39	chr4:122282200-122295600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:122283400-122284000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:122287600-122288400	Enhancers	Left Ventricle	heart
42	chr4:122290600-122290800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:122294000-122294200	Enhancers	HMEC	breast
44	chr4:122294000-122294800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr4:122294200-122294600	Weak transcription	HMEC	breast
46	chr4:122294600-122295000	Enhancers	HMEC	breast
47	chr4:122294800-122295200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr4:122294800-122298800	Enhancers	NHEK	skin
49	chr4:122295000-122295400	Flanking Active TSS	HMEC	breast
50	chr4:122295000-122295800	Enhancers	Fetal Lung	lung

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