Variant report

Variant	nsv879292
Chromosome Location	chr4:69382080-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:902)
CpG islands
(count:610)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:902 , 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	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
7	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
8	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
9	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
10	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
13	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
16	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
17	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
18	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
21	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
22	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
23	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
24	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
25	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
26	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
27	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
29	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
31	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
32	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
34	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
36	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
37	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
38	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
40	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
42	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
43	CTCF	chr4:69434820-69434970	GM12874	blood:	n/a	n/a
44	CTCF	chr4:69443425-69443543	GM12892	blood:	n/a	n/a
45	CTCF	chr4:69537096-69537228	GM12892	blood:	n/a	n/a
46	CTCF	chr4:69538995-69539098	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:69539160-69539310	GM12874	blood:	n/a	n/a
48	CTCF	chr4:69434820-69434970	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:69419753-69419990	GM19239	blood:	n/a	n/a
50	CTCF	chr4:69443360-69443510	GM12865	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537826-69537876	Caco-2	colon:	n/a
2	chr4:69537826-69537876	HIPEpiC	eye:	n/a
3	chr4:69536319-69536369	HCM	heart:	n/a
4	chr4:69537826-69537876	NB4	blood:	n/a
5	chr4:69537806-69537856	SK-N-SH	brain:	n/a
6	chr4:69434475-69434525	MCF10A-Er-Src	breast:	n/a
7	chr4:69514031-69514081	GM12891	blood:	n/a
8	chr4:69435593-69435643	HCPEpiC	choroid plexus:	n/a
9	chr4:69514031-69514081	MCF-7	breast:	n/a
10	chr4:69435601-69435651	NH-A	brain:	n/a
11	chr4:69536319-69536369	PANC-1	pancreas:	n/a
12	chr4:69514031-69514081	PFSK-1	brain:	n/a
13	chr4:69435250-69435300	AG04449	skin:	fetal
14	chr4:69536319-69536369	SK-N-SH	brain:	n/a
15	chr4:69435593-69435643	LNCaP	prostate:	n/a
16	chr4:69435250-69435300	A549	lung:	n/a
17	chr4:69537826-69537876	HRCEpiC	kidney:	n/a
18	chr4:69536319-69536369	HUVEC	blood vessel:	n/a
19	chr4:69536319-69536369	HRE	kidney:	n/a
20	chr4:69537806-69537856	HCF	heart:	n/a
21	chr4:69536319-69536369	BJ	skin:	n/a
22	chr4:69435601-69435651	HEEpiC	esophagus:	n/a
23	chr4:69434475-69434525	Caco-2	colon:	n/a
24	chr4:69514031-69514081	HRE	kidney:	n/a
25	chr4:69537589-69537639	PANC-1	pancreas:	n/a
26	chr4:69434475-69434525	AG09319	gingival:	n/a
27	chr4:69435250-69435300	NHBE	bronchial:	n/a
28	chr4:69514031-69514081	PANC-1	pancreas:	n/a
29	chr4:69434475-69434525	SK-N-MC	brain:	n/a
30	chr4:69435593-69435643	HMEC	breast:	n/a
31	chr4:69537806-69537856	K562	blood:	n/a
32	chr4:69537806-69537856	PANC-1	pancreas:	n/a
33	chr4:69514031-69514081	GM19239	blood:	n/a
34	chr4:69537826-69537876	HEK293	kidney:	embryo
35	chr4:69536319-69536369	HMEC	breast:	n/a
36	chr4:69536319-69536369	GM12891	blood:	n/a
37	chr4:69537589-69537639	HNPCEpiC	eye:	n/a
38	chr4:69537826-69537876	AG10803	skin:	n/a
39	chr4:69434475-69434525	PrEC	prostate:	n/a
40	chr4:69537826-69537876	RPTEC	kidney:	n/a
41	chr4:69537806-69537856	Caco-2	colon:	n/a
42	chr4:69537826-69537876	AG09309	skin:	n/a
43	chr4:69435601-69435651	GM12878	blood:	n/a
44	chr4:69434475-69434525	GM12878	blood:	n/a
45	chr4:69514031-69514081	CMK	blood:	n/a
46	chr4:69435593-69435643	NHBE	bronchial:	n/a
47	chr4:69536319-69536369	HepG2	liver:	n/a
48	chr4:69434475-69434525	BJ	skin:	n/a
49	chr4:69434475-69434525	MCF-7	breast:	n/a
50	chr4:69435593-69435643	HAEpiC	amniotic membrane:	n/a

(count:4 , 50 per page) page: 1

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

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

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

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: 5284 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5284 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371278809	chr4:69382645-69382646	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs557433311	chr4:69382671-69382672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs13127666	chr4:69382683-69382684	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs540257352	chr4:69382687-69382688	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs368029258	chr4:69382716-69382717	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs186321355	chr4:69382720-69382721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs10212906	chr4:69382729-69382730	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs376132526	chr4:69382733-69382734	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs10212950	chr4:69382734-69382735	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs10212951	chr4:69382748-69382749	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs10213260	chr4:69382805-69382806	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs10004899	chr4:69382863-69382864	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs570484603	chr4:69382868-69382869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs10213263	chr4:69382908-69382909	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546625594	chr4:69382943-69382944	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs191284200	chr4:69382953-69382954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs535994315	chr4:69382988-69382989	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs555227292	chr4:69383065-69383066	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs377460919	chr4:69383101-69383102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs537720495	chr4:69383123-69383124	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs183545658	chr4:69383168-69383169	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs73823662	chr4:69383179-69383180	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs187316253	chr4:69383196-69383197	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs146729535	chr4:69383211-69383212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs373779880	chr4:69383229-69383230	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs562108107	chr4:69383269-69383270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575818623	chr4:69383281-69383282	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs544508713	chr4:69383282-69383283	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs34107366	chr4:69383355-69383356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs12507161	chr4:69383356-69383357	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs66775684	chr4:69383357-69383358	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs34094476	chr4:69383360-69383361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs546588747	chr4:69383383-69383384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs560119557	chr4:69383411-69383412	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs12503212	chr4:69383431-69383432	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187921399	chr4:69383492-69383493	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs569279343	chr4:69383525-69383526	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557779965	chr4:69383550-69383551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs142615595	chr4:69384356-69384357	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs190406753	chr4:69384362-69384363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs4576087	chr4:69384363-69384364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs77609703	chr4:69384366-69384367	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs202039327	chr4:69384378-69384379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs4401527	chr4:69384380-69384381	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs151136672	chr4:69384397-69384398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527778086	chr4:69384440-69384441	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs547846317	chr4:69384455-69384456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs570233971	chr4:69384719-69384720	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs535720238	chr4:69384780-69384781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs116799448	chr4:69384836-69384837	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69388400-69389000	Enhancers	NHEK	skin
2	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
6	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
8	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
9	chr4:69403400-69404800	Strong transcription	Liver	Liver
10	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
13	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:69404800-69406800	Weak transcription	Liver	Liver
16	chr4:69405600-69406800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
17	chr4:69406200-69407000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr4:69406800-69407800	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr4:69406800-69409200	Strong transcription	Liver	Liver
20	chr4:69407000-69413800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:69407800-69408200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
22	chr4:69408200-69408600	Enhancers	HepG2	liver
23	chr4:69408200-69409200	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr4:69409200-69413600	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr4:69409200-69418800	Weak transcription	Liver	Liver
26	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr4:69417200-69418400	Enhancers	NHEK	skin
28	chr4:69417800-69418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:69417800-69419200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:69417800-69420600	Enhancers	HepG2	liver
31	chr4:69418600-69419200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr4:69418800-69419200	Enhancers	Liver	Liver
33	chr4:69418800-69421800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr4:69420600-69421000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:69421000-69423400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:69421600-69423000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr4:69421800-69422200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:69421800-69422600	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr4:69422200-69430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:69422400-69422800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:69422600-69431200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr4:69427200-69427400	Enhancers	Liver	Liver
43	chr4:69427400-69433200	Weak transcription	Liver	Liver
44	chr4:69429200-69439800	Weak transcription	Right Atrium	heart
45	chr4:69430400-69430800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:69431200-69431400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
47	chr4:69431200-69431600	Enhancers	HMEC	breast
48	chr4:69431400-69434600	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr4:69432800-69434200	Active TSS	Duodenum Mucosa	Duodenum
50	chr4:69433200-69433400	Flanking Active TSS	Liver	Liver

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