Variant report

Variant	nsv537149
Chromosome Location	chr4:80620595-80814456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:427)
Chromatin interactive
region (count:23)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80685291-80685539	K562	blood:	n/a	n/a
2	ATF1	chr4:80790831-80791068	K562	blood:	n/a	n/a
3	ATF1	chr4:80773436-80773735	K562	blood:	n/a	n/a
4	ATF1	chr4:80685309-80685612	K562	blood:	n/a	n/a
5	ATF1	chr4:80621566-80621751	K562	blood:	n/a	n/a
6	ATF1	chr4:80792382-80792496	K562	blood:	n/a	n/a
7	BATF	chr4:80681049-80681323	GM12878	blood:	n/a	chr4:80681190-80681201
8	BATF	chr4:80681101-80681304	GM12878	blood:	n/a	chr4:80681190-80681201
9	BRCA1	chr4:80807403-80807424	GM12878	blood:	n/a	n/a
10	CBX3	chr4:80710056-80710422	K562	blood:	n/a	n/a
11	CBX3	chr4:80799340-80799593	K562	blood:	n/a	n/a
12	CBX3	chr4:80688764-80689088	K562	blood:	n/a	n/a
13	CBX3	chr4:80710064-80710413	K562	blood:	n/a	n/a
14	CEBPB	chr4:80773350-80773719	K562	blood:	n/a	n/a
15	CEBPB	chr4:80773370-80773613	K562	blood:	n/a	n/a
16	CEBPB	chr4:80773247-80773927	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:80731564-80731880	HepG2	liver:	n/a	chr4:80731709-80731720
18	CEBPB	chr4:80731548-80731883	IMR90	lung:	n/a	chr4:80731709-80731720
19	CEBPB	chr4:80706714-80706914	A549	lung:	n/a	chr4:80706790-80706801
20	CEBPB	chr4:80784213-80784244	K562	blood:	n/a	n/a
21	CEBPB	chr4:80773356-80773708	K562	blood:	n/a	n/a
22	CEBPB	chr4:80773198-80773899	HCT-116	colon:	n/a	n/a
23	CEBPB	chr4:80741218-80741326	A549	lung:	n/a	chr4:80741308-80741321 chr4:80741310-80741321 chr4:80741308-80741321
24	CEBPB	chr4:80771303-80771333	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:80725691-80725968	HepG2	liver:	n/a	chr4:80725802-80725813
26	CEBPB	chr4:80706633-80706957	IMR90	lung:	n/a	chr4:80706790-80706801
27	CEBPB	chr4:80773387-80773711	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:80773353-80773733	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:80621582-80621882	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:80772769-80773720	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:80772730-80773792	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:80806605-80806770	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:80621616-80621838	K562	blood:	n/a	n/a
34	CEBPB	chr4:80741210-80741367	K562	blood:	n/a	chr4:80741308-80741321 chr4:80741310-80741321 chr4:80741308-80741321
35	CEBPB	chr4:80685475-80685488	K562	blood:	n/a	n/a
36	CEBPB	chr4:80706630-80706962	HepG2	liver:	n/a	chr4:80706790-80706801
37	CEBPB	chr4:80769907-80770099	HepG2	liver:	n/a	chr4:80769965-80769978
38	CEBPB	chr4:80767481-80767657	K562	blood:	n/a	chr4:80767540-80767553 chr4:80767573-80767586 chr4:80767542-80767553 chr4:80767542-80767551
39	CEBPB	chr4:80779116-80779132	HepG2	liver:	n/a	n/a
40	CEBPD	chr4:80685349-80685623	K562	blood:	n/a	n/a
41	CHD2	chr4:80655647-80655866	K562	blood:	n/a	n/a
42	CTCF	chr4:80684849-80684871	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:80741720-80741870	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:80741740-80741890	GM12878	blood:	n/a	n/a
45	CTCF	chr4:80684792-80684899	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:80683560-80683710	AG09319	gingival:	n/a	n/a
47	CTCF	chr4:80724575-80724649	GM20000	blood:	n/a	n/a
48	CTCF	chr4:80684800-80684950	GM12866	blood:	n/a	n/a
49	CTCF	chr4:80764285-80764300	GM20000	blood:	n/a	n/a
50	CTCF	chr4:80661160-80661310	GM06990	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80748552-80748602	HCM	heart:	n/a
2	chr4:80748552-80748602	IMR90	lung:	fetal
3	chr4:80747387-80747437	H1-hESC	embryonic stem cell:	embryo
4	chr4:80644890-80644940	AG10803	skin:	n/a
5	chr4:80786707-80786757	HUVEC	blood vessel:	n/a
6	chr4:80748552-80748602	AG09319	gingival:	n/a
7	chr4:80747387-80747437	HUVEC	blood vessel:	n/a
8	chr4:80748660-80748710	HMEC	breast:	n/a
9	chr4:80786707-80786757	U87	brain:	n/a
10	chr4:80747125-80747175	NHDF-neo	bronchial:	n/a
11	chr4:80747387-80747437	A549	lung:	n/a
12	chr4:80748660-80748710	SK-N-SH	brain:	n/a
13	chr4:80747125-80747175	HCM	heart:	n/a
14	chr4:80747387-80747437	HepG2	liver:	n/a
15	chr4:80748660-80748710	AG09309	skin:	n/a
16	chr4:80775399-80775449	HAEpiC	amniotic membrane:	n/a
17	chr4:80748552-80748602	LNCaP	prostate:	n/a
18	chr4:80748552-80748602	Caco-2	colon:	n/a
19	chr4:80748552-80748602	K562	blood:	n/a
20	chr4:80644890-80644940	HRPEpiC	eye:	n/a
21	chr4:80748660-80748710	Hela-S3	cervix:	n/a
22	chr4:80747125-80747175	HCT-116	colon:	n/a
23	chr4:80644890-80644940	NB4	blood:	n/a
24	chr4:80748660-80748710	SKMC	muscle:	n/a
25	chr4:80786707-80786757	HEK293	kidney:	embryo
26	chr4:80786707-80786757	ECC-1	luminal epithelium:	n/a
27	chr4:80775399-80775449	BJ	skin:	n/a
28	chr4:80747125-80747175	Caco-2	colon:	n/a
29	chr4:80747125-80747175	BE2_C	brain:	n/a
30	chr4:80748660-80748710	HCPEpiC	choroid plexus:	n/a
31	chr4:80748660-80748710	HRCEpiC	kidney:	n/a
32	chr4:80747387-80747437	HRE	kidney:	n/a
33	chr4:80786707-80786757	HEEpiC	esophagus:	n/a
34	chr4:80775399-80775449	ProgFib	skin:	n/a
35	chr4:80786707-80786757	ProgFib	skin:	n/a
36	chr4:80644890-80644940	Caco-2	colon:	n/a
37	chr4:80748660-80748710	NHDF-neo	bronchial:	n/a
38	chr4:80748552-80748602	HRPEpiC	eye:	n/a
39	chr4:80644890-80644940	HCPEpiC	choroid plexus:	n/a
40	chr4:80748552-80748602	AoSMC	blood vessel:	n/a
41	chr4:80747387-80747437	Hela-S3	cervix:	n/a
42	chr4:80786707-80786757	PANC-1	pancreas:	n/a
43	chr4:80747387-80747437	MCF10A-Er-Src	breast:	n/a
44	chr4:80775399-80775449	HUVEC	blood vessel:	n/a
45	chr4:80644890-80644940	NHDF-neo	bronchial:	n/a
46	chr4:80748660-80748710	PFSK-1	brain:	n/a
47	chr4:80747387-80747437	IMR90	lung:	fetal
48	chr4:80748552-80748602	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:80775399-80775449	SAEC	small airway:	n/a
50	chr4:80747125-80747175	GM12891	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
2	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
3	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
4	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
5	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
6	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
7	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
8	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
9	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
10	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
11	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
12	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
13	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
14	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
15	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
16	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
17	chr4:80799782..80802342-chr4:80814982..80816736,2	K562	blood:
18	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
19	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
20	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
21	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
22	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
23	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-1	chr4:80782444-80784401	ENSG00000251321.1
2	lnc-PRDM8-7	chr4:80763406-80763602	l_2676_chr4:80740905-80762602_adipose
3	lnc-PRDM8-7	chr4:80751264-80751305	l_2676_chr4:80740905-80762602_adipose
4	lnc-PRDM8-1	chr4:80748625-80748757	ENSG00000251321.1
5	lnc-PRDM8-1	chr4:80748689-80748757	ENSG00000251321.1
6	lnc-PRDM8-8	chr4:80633330-80633763	ucscGeneNc_uc003hlv_2
7	lnc-PRDM8-7	chr4:80747007-80747134	l_2676_chr4:80740905-80762602_adipose
8	lnc-PRDM8-8	chr4:80632771-80632952	ucscGeneNc_uc003hlv_2
9	lnc-PRDM8-1	chr4:80798769-80798924	ENSG00000251321.1
10	lnc-PRDM8-8	chr4:80715319-80716636	ucscGeneNc_uc003hlv_2
11	lnc-PRDM8-1	chr4:80782444-80782591	ENSG00000251321.1
12	lnc-PRDM8-8	chr4:80653963-80654080	ucscGeneNc_uc003hlv_2
13	lnc-PRDM8-7	chr4:80740906-80740955	l_2676_chr4:80740905-80762602_adipose
14	lnc-PRDM8-7	chr4:80762510-80762602	l_2676_chr4:80740905-80762602_adipose

No data

Variant related genes	Relation type
ENSG00000212620	TF binding region
PCAT4	TF binding region
ENSG00000212620	CpG island
PCAT4	CpG island

Extended variants
information (count: 3713 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3713 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201386164	chr4:80622020-80622021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559376546	chr4:80622045-80622046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115579255	chr4:80622080-80622081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145010585	chr4:80622086-80622087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186199044	chr4:80622129-80622130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537290077	chr4:80622135-80622136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560877222	chr4:80622137-80622138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551245632	chr4:80622217-80622218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567870930	chr4:80622247-80622248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536196525	chr4:80622286-80622287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553024283	chr4:80622340-80622341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545023566	chr4:80622349-80622350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80060903	chr4:80622359-80622360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368748120	chr4:80622364-80622365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553694236	chr4:80623426-80623427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553422869	chr4:80623467-80623468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558596644	chr4:80623472-80623473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572889717	chr4:80623475-80623476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545008754	chr4:80623476-80623477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564989190	chr4:80623498-80623499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542694978	chr4:80623516-80623517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201509013	chr4:80623518-80623519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530929182	chr4:80623592-80623593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544756456	chr4:80623595-80623596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72649385	chr4:80625410-80625411	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546160876	chr4:80625416-80625417	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs111302432	chr4:80625558-80625559	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs184025760	chr4:80625562-80625563	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548169348	chr4:80625573-80625574	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561416746	chr4:80625631-80625632	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs527399231	chr4:80625660-80625661	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187737046	chr4:80625662-80625663	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs550701076	chr4:80625670-80625671	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs189927114	chr4:80625720-80625721	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs533005286	chr4:80625736-80625737	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs28591595	chr4:80625737-80625738	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569944095	chr4:80625740-80625741	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537804161	chr4:80625741-80625742	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554971803	chr4:80625757-80625758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs568533402	chr4:80625775-80625776	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536690930	chr4:80632829-80632830	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs539432554	chr4:80632856-80632857	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs557537889	chr4:80632873-80632874	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs114561958	chr4:80632918-80632919	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs9999607	chr4:80632920-80632921	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs542806683	chr4:80632929-80632930	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs576113076	chr4:80633364-80633365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs78672340	chr4:80633386-80633387	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs4975111	chr4:80633389-80633390	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571858646	chr4:80633430-80633431	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
lymphocytic leukemia	21291569	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
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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80622000-80622400	Enhancers	Placenta	Placenta
2	chr4:80623400-80623600	Enhancers	Aorta	Aorta
3	chr4:80625400-80625800	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr4:80635000-80635400	Enhancers	Colon Smooth Muscle	Colon
5	chr4:80636000-80636200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:80636200-80644800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:80642000-80642600	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr4:80642200-80642600	Enhancers	Rectal Smooth Muscle	rectum
9	chr4:80642200-80642600	Active TSS	Stomach Smooth Muscle	stomach
10	chr4:80644600-80644800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:80644600-80645200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:80644600-80645200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:80644600-80645400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:80644800-80645000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr4:80644800-80645000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:80644800-80645000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:80644800-80645200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr4:80644800-80645200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:80645000-80645200	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr4:80657800-80658000	Enhancers	Placenta	Placenta
21	chr4:80658400-80661000	Weak transcription	Placenta	Placenta
22	chr4:80660600-80661400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:80661000-80661200	Enhancers	Placenta	Placenta
24	chr4:80661000-80661400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:80661000-80661600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:80661200-80661600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:80663600-80664000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:80663600-80664400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:80669000-80669200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:80669400-80671000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:80669800-80670200	Enhancers	Placenta	Placenta
32	chr4:80670000-80670200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:80670000-80670400	Enhancers	Pancreas	Pancrea
34	chr4:80670000-80670400	Enhancers	K562	blood
35	chr4:80671000-80671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:80671200-80672000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:80675400-80675800	Enhancers	Colon Smooth Muscle	Colon
38	chr4:80675800-80676600	Enhancers	Rectal Smooth Muscle	rectum
39	chr4:80675800-80677600	Weak transcription	Colon Smooth Muscle	Colon
40	chr4:80676600-80677800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr4:80677200-80677600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:80677600-80678800	Enhancers	Colon Smooth Muscle	Colon
43	chr4:80677800-80678800	Enhancers	Rectal Smooth Muscle	rectum
44	chr4:80678200-80679000	Enhancers	Placenta Amnion	Placenta Amnion
45	chr4:80678200-80679400	Enhancers	Placenta	Placenta
46	chr4:80678600-80679400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:80678800-80679400	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr4:80683200-80683600	Enhancers	Dnd41	blood
49	chr4:80684800-80685400	Enhancers	K562	blood
50	chr4:80685600-80685800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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