Variant report

Variant	esv1010272
Chromosome Location	chr4:74802868-74813081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:72)
CpG islands
(count:367)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:72 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr4:74810327-74810502	K562	blood:	n/a	n/a
2	CTCF	chr4:74809880-74810030	HPF	lung:	n/a	n/a
3	CTCF	chr4:74809900-74810050	HCM	heart:	n/a	chr4:74810025-74810038
4	CTCF	chr4:74809902-74810110	NHEK	skin:	n/a	chr4:74810025-74810038
5	CTCF	chr4:74809880-74810030	HRPEpiC	eye:	n/a	n/a
6	CTCF	chr4:74809900-74810050	AG04449	skin:	n/a	chr4:74810025-74810038
7	CTCF	chr4:74809960-74810110	HCFaa	heart:	n/a	chr4:74810025-74810038
8	CTCF	chr4:74809980-74810130	HAc	cerebellar:	n/a	chr4:74810025-74810038
9	CTCF	chr4:74809920-74810070	HRE	kidney:	n/a	chr4:74810025-74810038
10	CTCF	chr4:74809920-74810070	HCPEpiC	choroid plexus:	n/a	chr4:74810025-74810038
11	CTCF	chr4:74809960-74810110	HRE	kidney:	n/a	chr4:74810025-74810038
12	CTCF	chr4:74809900-74810050	HMF	breast:	n/a	chr4:74810025-74810038
13	CTCF	chr4:74809954-74810045	Medullo	brain:	n/a	chr4:74810025-74810038
14	CTCF	chr4:74809964-74810025	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:74809900-74810050	AG09319	gingival:	n/a	chr4:74810025-74810038
16	CTCF	chr4:74809900-74810050	RPTEC	kidney:	n/a	chr4:74810025-74810038
17	CTCF	chr4:74804657-74804690	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr4:74809800-74809950	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:74809940-74810090	HBMEC	blood vessel:	n/a	chr4:74810025-74810038
20	CTCF	chr4:74809983-74810009	A549	lung:	n/a	n/a
21	CTCF	chr4:74811982-74812009	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr4:74809960-74810080	Fibrobl	skin:	n/a	chr4:74810025-74810038
23	CTCF	chr4:74809920-74810070	HRPEpiC	eye:	n/a	chr4:74810025-74810038
24	CTCF	chr4:74809880-74810030	SAEC	small airway:	n/a	n/a
25	CTCF	chr4:74809940-74810090	HPAF	blood vessel:	n/a	chr4:74810025-74810038
26	CTCF	chr4:74809880-74810030	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr4:74809960-74810110	HUVEC	blood vessel:	n/a	chr4:74810025-74810038
28	CTCF	chr4:74809960-74810110	HCM	heart:	n/a	chr4:74810025-74810038
29	CTCF	chr4:74809860-74810010	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr4:74809955-74810052	ProgFib	skin:	n/a	chr4:74810025-74810038
31	CTCF	chr4:74809960-74810110	HFF-Myc	foreskin:	n/a	chr4:74810025-74810038
32	CTCF	chr4:74809900-74810050	HFF	foreskin:	n/a	chr4:74810025-74810038
33	E2F4	chr4:74810318-74810699	MCF10A-Er-Src	breast:	n/a	n/a
34	EGR1	chr4:74810112-74810561	K562	blood:	n/a	chr4:74810260-74810275 chr4:74810274-74810281
35	EGR1	chr4:74810251-74810573	ECC-1	luminal epithelium:	n/a	chr4:74810260-74810275 chr4:74810274-74810281
36	EGR1	chr4:74810102-74810567	K562	blood:	n/a	chr4:74810260-74810275 chr4:74810274-74810281
37	ELK4	chr4:74806918-74807024	HEK293	kidney:	n/a	n/a
38	EP300	chr4:74807662-74807777	K562	blood:	n/a	n/a
39	FAM48A	chr4:74808478-74808589	GM12878	blood:	n/a	n/a
40	FOS	chr4:74806577-74806703	MCF10A-Er-Src	breast:	n/a	n/a
41	HDAC2	chr4:74809202-74809680	H1-hESC	embryonic stem cell:	n/a	n/a
42	HMGN3	chr4:74809824-74810071	K562	blood:	n/a	n/a
43	JUND	chr4:74809988-74810022	H1-hESC	embryonic stem cell:	n/a	n/a
44	KAP1	chr4:74810689-74811533	HEK293	kidney:	n/a	chr4:74811299-74811307
45	MAFF	chr4:74810585-74810650	K562	blood:	n/a	n/a
46	MAFK	chr4:74810522-74810644	HepG2	liver:	n/a	chr4:74810596-74810611
47	MAFK	chr4:74810490-74810728	IMR90	lung:	n/a	chr4:74810596-74810611
48	MAFK	chr4:74806263-74806344	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAFK	chr4:74810519-74810719	HepG2	liver:	n/a	chr4:74810596-74810611
50	MAX	chr4:74810278-74810553	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74810310-74810360	AoSMC	blood vessel:	n/a
2	chr4:74810310-74810360	AoSMC	blood vessel:	n/a
3	chr4:74810017-74810067	HL-60	blood:	n/a
4	chr4:74810310-74810360	HIPEpiC	eye:	n/a
5	chr4:74810142-74810192	Jurkat	blood:	n/a
6	chr4:74810142-74810192	HCPEpiC	choroid plexus:	n/a
7	chr4:74809912-74809962	AG04449	skin:	fetal
8	chr4:74810017-74810067	NH-A	brain:	n/a
9	chr4:74810310-74810360	HMEC	breast:	n/a
10	chr4:74809912-74809962	NB4	blood:	n/a
11	chr4:74810310-74810360	AG04449	skin:	fetal
12	chr4:74806905-74806955	AG09319	gingival:	n/a
13	chr4:74810017-74810067	SK-N-SH_RA	brain:	n/a
14	chr4:74808337-74808387	Hela-S3	cervix:	n/a
15	chr4:74808337-74808387	SK-N-SH_RA	brain:	n/a
16	chr4:74808337-74808387	NHDF-neo	bronchial:	n/a
17	chr4:74810142-74810192	Hela-S3	cervix:	n/a
18	chr4:74810017-74810067	GM12892	blood:	n/a
19	chr4:74810142-74810192	AG09319	gingival:	n/a
20	chr4:74809912-74809962	NHBE	bronchial:	n/a
21	chr4:74810142-74810192	IMR90	lung:	fetal
22	chr4:74810310-74810360	SK-N-MC	brain:	n/a
23	chr4:74806905-74806955	ProgFib	skin:	n/a
24	chr4:74809912-74809962	HEK293	kidney:	embryo
25	chr4:74806905-74806955	SK-N-SH	brain:	n/a
26	chr4:74808337-74808387	HUVEC	blood vessel:	n/a
27	chr4:74808337-74808387	ovcar-3	ovarian:	n/a
28	chr4:74810310-74810360	HCM	heart:	n/a
29	chr4:74810017-74810067	NHDF-neo	bronchial:	n/a
30	chr4:74810017-74810067	SK-N-MC	brain:	n/a
31	chr4:74808337-74808387	AoSMC	blood vessel:	n/a
32	chr4:74809912-74809962	AoSMC	blood vessel:	n/a
33	chr4:74810310-74810360	K562	blood:	n/a
34	chr4:74809912-74809962	K562	blood:	n/a
35	chr4:74810017-74810067	HIPEpiC	eye:	n/a
36	chr4:74810310-74810360	HCPEpiC	choroid plexus:	n/a
37	chr4:74810017-74810067	U87	brain:	n/a
38	chr4:74810310-74810360	NHBE	bronchial:	n/a
39	chr4:74810142-74810192	T-47D	breast:	n/a
40	chr4:74810142-74810192	HCF	heart:	n/a
41	chr4:74806905-74806955	U87	brain:	n/a
42	chr4:74810142-74810192	NHDF-neo	bronchial:	n/a
43	chr4:74810017-74810067	BE2_C	brain:	n/a
44	chr4:74810142-74810192	GM12891	blood:	n/a
45	chr4:74810310-74810360	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:74806905-74806955	HRPEpiC	eye:	n/a
47	chr4:74809912-74809962	HCM	heart:	n/a
48	chr4:74810310-74810360	HEEpiC	esophagus:	n/a
49	chr4:74810017-74810067	GM06990	blood:	n/a
50	chr4:74810310-74810360	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:74801511..74803717-chr4:74807849..74809855,2	K562	blood:
2	chr4:74800982..74803717-chr4:74808355..74810673,2	K562	blood:
3	chr4:74803360..74804892-chr4:74805516..74807150,2	K562	blood:
4	chr4:74803360..74804892-chr4:74805516..74807150,2	K562	blood:
5	chr4:74806189..74808887-chr4:74899171..74901501,2	K562	blood:
6	chr4:74801511..74803717-chr4:74807849..74809855,2	K562	blood:

No data

Variant related genes	Relation type
CXCL1P	TF binding region
HNRNPA1P55	TF binding region
CXCL1P	CpG island
HNRNPA1P55	CpG island
ENSG00000250339	chromatin interactions

Extended variants
information (count: 403 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561008778	chr4:74802887-74802888	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs377075000	chr4:74802967-74802968	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550951018	chr4:74803061-74803062	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112303453	chr4:74803098-74803099	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562686148	chr4:74803100-74803101	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs137855615	chr4:74803128-74803129	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs142369627	chr4:74803236-74803237	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566208301	chr4:74803269-74803270	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548376636	chr4:74803385-74803386	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570555381	chr4:74803386-74803387	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562170120	chr4:74803388-74803389	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371304000	chr4:74803393-74803394	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533623377	chr4:74803425-74803426	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181419947	chr4:74803434-74803435	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552264155	chr4:74803556-74803557	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151265610	chr4:74803564-74803565	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527797860	chr4:74803565-74803566	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537849746	chr4:74803568-74803569	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556491773	chr4:74803617-74803618	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370300052	chr4:74803648-74803649	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs352020	chr4:74803650-74803651	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs530607208	chr4:74803653-74803654	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548798437	chr4:74803693-74803694	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554040407	chr4:74803697-74803698	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367859452	chr4:74803718-74803719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76991297	chr4:74803735-74803736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538906355	chr4:74803750-74803751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540335592	chr4:74803769-74803770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529333930	chr4:74803776-74803777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186002832	chr4:74803802-74803803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149707021	chr4:74803859-74803860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191095943	chr4:74803891-74803892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367720820	chr4:74803951-74803952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562833200	chr4:74803954-74803955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530354896	chr4:74803990-74803991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548493351	chr4:74803992-74803993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144634713	chr4:74803993-74803994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2367438	chr4:74803994-74803995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2367439	chr4:74803995-74803996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371673031	chr4:74804011-74804012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570571699	chr4:74804044-74804045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150472558	chr4:74804059-74804060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537430572	chr4:74804063-74804064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs386676054	chr4:74804066-74804067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549833125	chr4:74804067-74804068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568343740	chr4:74804088-74804089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535721189	chr4:74804097-74804098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183459692	chr4:74804102-74804103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569073856	chr4:74804105-74804106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185926771	chr4:74804196-74804197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-small cell lung cancer	21829676	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74802400-74803200	Enhancers	Fetal Intestine Large	intestine
2	chr4:74802600-74803400	Enhancers	A549	lung
3	chr4:74803000-74803600	Enhancers	Duodenum Mucosa	Duodenum
4	chr4:74803400-74803600	Enhancers	Stomach Mucosa	stomach
5	chr4:74803400-74803800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:74803800-74809000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:74806000-74806600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:74806200-74806400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:74806600-74807400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:74807800-74808000	Enhancers	K562	blood
11	chr4:74808200-74809400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr4:74808400-74809600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr4:74808400-74809600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:74808400-74809800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr4:74808400-74809800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:74808600-74809200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr4:74808600-74809600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr4:74809000-74809200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
19	chr4:74809000-74809200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
20	chr4:74809000-74809400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:74809000-74809400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr4:74809000-74809600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
23	chr4:74809000-74810000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:74809200-74809400	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
25	chr4:74809200-74809600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
26	chr4:74809200-74809600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
27	chr4:74809200-74809800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
28	chr4:74809200-74809800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:74809200-74809800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:74809400-74809600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:74809400-74809600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:74809400-74809600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:74809400-74809600	Enhancers	HUVEC	blood vessel
34	chr4:74809400-74809800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
35	chr4:74809400-74809800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
36	chr4:74809400-74810400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
37	chr4:74809600-74809800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:74809600-74809800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:74809600-74809800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:74809600-74809800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
41	chr4:74809600-74809800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:74809600-74809800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:74809600-74809800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:74809600-74809800	Bivalent Enhancer	Brain Anterior Caudate	brain
45	chr4:74809600-74809800	Bivalent Enhancer	Brain Germinal Matrix	brain
46	chr4:74809600-74809800	Enhancers	Pancreas	Pancrea
47	chr4:74809600-74809800	Enhancers	HMEC	breast
48	chr4:74809600-74809800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
49	chr4:74809600-74809800	Flanking Bivalent TSS/Enh	NHEK	skin
50	chr4:74809600-74810000	Bivalent Enhancer	Fetal Intestine Small	intestine

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