Variant report

Variant	nsv1010888
Chromosome Location	chr4:69371991-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:924)
CpG islands
(count:675)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
7	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
8	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
10	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
11	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
12	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
13	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
16	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
17	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
19	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
20	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
21	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
22	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
23	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
24	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
25	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
26	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
28	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
29	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
30	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
32	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
36	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
37	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
38	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
39	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
41	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
42	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
43	CTCF	chr4:69534366-69534476	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr4:69538940-69539090	K562	blood:	n/a	n/a
45	CTCF	chr4:69537040-69537297	GM19238	blood:	n/a	n/a
46	CTCF	chr4:69523079-69523241	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:69537020-69537170	HEK293	kidney:	n/a	n/a
48	CTCF	chr4:69434889-69435082	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:69537040-69537190	GM12871	blood:	n/a	n/a
50	CTCF	chr4:69419874-69419947	Kidney_OC	kidney:	n/a	n/a

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69514031-69514081	BE2_C	brain:	n/a
2	chr4:69435250-69435300	HAEpiC	amniotic membrane:	n/a
3	chr4:69381368-69381418	NH-A	brain:	n/a
4	chr4:69537806-69537856	BJ	skin:	n/a
5	chr4:69514031-69514081	BE2_C	brain:	n/a
6	chr4:69435250-69435300	HAEpiC	amniotic membrane:	n/a
7	chr4:69381368-69381418	NH-A	brain:	n/a
8	chr4:69537806-69537856	BJ	skin:	n/a
9	chr4:69434475-69434525	HAEpiC	amniotic membrane:	n/a
10	chr4:69537806-69537856	Hepatocyte	liver:	n/a
11	chr4:69435593-69435643	Jurkat	blood:	n/a
12	chr4:69435250-69435300	GM12892	blood:	n/a
13	chr4:69537589-69537639	HNPCEpiC	eye:	n/a
14	chr4:69435593-69435643	HNPCEpiC	eye:	n/a
15	chr4:69537826-69537876	HepG2	liver:	n/a
16	chr4:69435601-69435651	HRE	kidney:	n/a
17	chr4:69435593-69435643	SKMC	muscle:	n/a
18	chr4:69435593-69435643	T-47D	breast:	n/a
19	chr4:69435250-69435300	K562	blood:	n/a
20	chr4:69537806-69537856	ECC-1	luminal epithelium:	n/a
21	chr4:69536319-69536369	CMK	blood:	n/a
22	chr4:69537589-69537639	PFSK-1	brain:	n/a
23	chr4:69514031-69514081	SK-N-MC	brain:	n/a
24	chr4:69514031-69514081	Caco-2	colon:	n/a
25	chr4:69435593-69435643	SAEC	small airway:	n/a
26	chr4:69434475-69434525	SK-N-SH_RA	brain:	n/a
27	chr4:69435593-69435643	A549	lung:	n/a
28	chr4:69435250-69435300	PrEC	prostate:	n/a
29	chr4:69536319-69536369	SKMC	muscle:	n/a
30	chr4:69536319-69536369	GM12878	blood:	n/a
31	chr4:69434475-69434525	ProgFib	skin:	n/a
32	chr4:69522639-69522689	HUVEC	blood vessel:	n/a
33	chr4:69435601-69435651	U87	brain:	n/a
34	chr4:69514031-69514081	SK-N-SH_RA	brain:	n/a
35	chr4:69537806-69537856	HAEpiC	amniotic membrane:	n/a
36	chr4:69381368-69381418	AoSMC	blood vessel:	n/a
37	chr4:69435601-69435651	Caco-2	colon:	n/a
38	chr4:69435593-69435643	BJ	skin:	n/a
39	chr4:69435601-69435651	AG09309	skin:	n/a
40	chr4:69537806-69537856	HEEpiC	esophagus:	n/a
41	chr4:69522639-69522689	SK-N-SH	brain:	n/a
42	chr4:69537826-69537876	NT2-D1	testis:	n/a
43	chr4:69435250-69435300	SK-N-MC	brain:	n/a
44	chr4:69435601-69435651	NHDF-neo	bronchial:	n/a
45	chr4:69514031-69514081	HRPEpiC	eye:	n/a
46	chr4:69537589-69537639	SK-N-MC	brain:	n/a
47	chr4:69537589-69537639	AG10803	skin:	n/a
48	chr4:69522639-69522689	SK-N-MC	brain:	n/a
49	chr4:69537806-69537856	PrEC	prostate:	n/a
50	chr4:69435601-69435651	Hepatocyte	liver:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
2	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
3	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
4	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
5	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
2	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
5	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
6	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000248635	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000248635	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island

Extended variants
information (count: 5402 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5402 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2708662	chr4:69371991-69371992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138233827	chr4:69372003-69372004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201535428	chr4:69372072-69372073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186999977	chr4:69372081-69372082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35057908	chr4:69372082-69372083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550305607	chr4:69372083-69372084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563303959	chr4:69372107-69372108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34595700	chr4:69372116-69372117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs552112173	chr4:69372138-69372139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535520093	chr4:69372182-69372183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs202015552	chr4:69372183-69372184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35833259	chr4:69372191-69372192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534649966	chr4:69372204-69372205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547777963	chr4:69372216-69372217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192389551	chr4:69372219-69372220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182438611	chr4:69372238-69372239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536710763	chr4:69372242-69372243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2708661	chr4:69372252-69372253	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576535192	chr4:69372259-69372260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2045097	chr4:69372321-69372322	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs558921348	chr4:69372341-69372342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377197921	chr4:69372342-69372343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9884390	chr4:69373407-69373408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546391555	chr4:69373411-69373412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566248180	chr4:69373432-69373433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535207296	chr4:69373456-69373457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141990358	chr4:69373474-69373475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2603149	chr4:69373476-69373477	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191961830	chr4:69373481-69373482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77333185	chr4:69373483-69373484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75207461	chr4:69373485-69373486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11941105	chr4:69373524-69373525	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371281236	chr4:69373532-69373533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577353739	chr4:69373553-69373554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76636647	chr4:69373554-69373555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185653799	chr4:69373586-69373587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62317939	chr4:69373588-69373589	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs144346078	chr4:69373628-69373629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368065461	chr4:69373632-69373633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544183639	chr4:69373659-69373660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564071239	chr4:69373667-69373668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532810135	chr4:69373668-69373669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546602416	chr4:69373728-69373729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148759739	chr4:69373758-69373759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139260944	chr4:69373763-69373764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370878539	chr4:69373842-69373843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3109121	chr4:69373846-69373847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9884394	chr4:69373864-69373865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs386675591	chr4:69373873-69373874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9884396	chr4:69373874-69373875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69370800-69372000	Weak transcription	Liver	Liver
2	chr4:69371200-69372200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr4:69372200-69372400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr4:69373400-69373800	Enhancers	Fetal Heart	heart
5	chr4:69373800-69374200	Weak transcription	Fetal Heart	heart
6	chr4:69374200-69375200	Enhancers	Fetal Heart	heart
7	chr4:69388400-69389000	Enhancers	NHEK	skin
8	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
12	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
14	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
15	chr4:69403400-69404800	Strong transcription	Liver	Liver
16	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
19	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:69404800-69406800	Weak transcription	Liver	Liver
22	chr4:69405600-69406800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
23	chr4:69406200-69407000	Strong transcription	Duodenum Mucosa	Duodenum
24	chr4:69406800-69407800	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr4:69406800-69409200	Strong transcription	Liver	Liver
26	chr4:69407000-69413800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr4:69407800-69408200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
28	chr4:69408200-69408600	Enhancers	HepG2	liver
29	chr4:69408200-69409200	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr4:69409200-69413600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:69409200-69418800	Weak transcription	Liver	Liver
32	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr4:69417200-69418400	Enhancers	NHEK	skin
34	chr4:69417800-69418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:69417800-69419200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:69417800-69420600	Enhancers	HepG2	liver
37	chr4:69418600-69419200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:69418800-69419200	Enhancers	Liver	Liver
39	chr4:69418800-69421800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr4:69420600-69421000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:69421000-69423400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:69421600-69423000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr4:69421800-69422200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:69421800-69422600	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr4:69422200-69430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:69422400-69422800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:69422600-69431200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr4:69427200-69427400	Enhancers	Liver	Liver
49	chr4:69427400-69433200	Weak transcription	Liver	Liver
50	chr4:69429200-69439800	Weak transcription	Right Atrium	heart

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