Variant report

Variant	nsv870554
Chromosome Location	chr1:74678285-74804833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:74710842-74711284	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:74710792-74711328	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:74721367-74721402	K562	blood:	n/a	n/a
4	BACH1	chr1:74721725-74721860	K562	blood:	n/a	n/a
5	BCL11A	chr1:74710899-74711179	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr1:74710883-74711156	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:74746472-74746612	K562	blood:	n/a	n/a
8	CEBPB	chr1:74777395-74777659	HepG2	liver:	n/a	chr1:74777540-74777553 chr1:74777541-74777552
9	CEBPB	chr1:74714756-74714989	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:74783464-74783590	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:74768320-74768669	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:74729369-74729404	H1-hESC	embryonic stem cell:	n/a	chr1:74729392-74729403
13	CEBPB	chr1:74764993-74765325	A549	lung:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
14	CEBPB	chr1:74780245-74780491	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:74771504-74771688	HepG2	liver:	n/a	chr1:74771612-74771623
16	CEBPB	chr1:74710897-74711276	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr1:74783362-74783693	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:74780146-74780463	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:74728463-74728579	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:74764987-74765324	HepG2	liver:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
21	CEBPZ	chr1:74790846-74791124	HepG2	liver:	n/a	n/a
22	CTCF	chr1:74737400-74737550	HMEC	breast:	n/a	n/a
23	CTCF	chr1:74761842-74761913	Fibrobl	skin:	n/a	n/a
24	CTCF	chr1:74737320-74737470	GM12864	blood:	n/a	n/a
25	CTCF	chr1:74737140-74737290	HCT-116	colon:	n/a	n/a
26	CTCF	chr1:74737320-74737470	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:74737280-74737430	HepG2	liver:	n/a	n/a
28	CTCF	chr1:74737355-74737375	GM20000	blood:	n/a	n/a
29	CTCF	chr1:74737300-74737450	HRE	kidney:	n/a	n/a
30	CTCF	chr1:74790800-74790950	HepG2	liver:	n/a	n/a
31	CTCF	chr1:74779180-74779330	HAc	cerebellar:	n/a	n/a
32	CTCF	chr1:74724669-74724758	K562	blood:	n/a	n/a
33	CTCF	chr1:74737340-74737490	HepG2	liver:	n/a	n/a
34	CTCF	chr1:74737260-74737410	HEK293	kidney:	n/a	n/a
35	CTCF	chr1:74737240-74737390	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr1:74802103-74802213	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr1:74737347-74737405	GM19239	blood:	n/a	n/a
38	CTCF	chr1:74737293-74737455	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:74737280-74737430	GM12873	blood:	n/a	n/a
40	CTCF	chr1:74737378-74737427	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:74737280-74737430	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:74737355-74737403	HepG2	liver:	n/a	n/a
43	CTCF	chr1:74737315-74737416	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:74737346-74737388	GM12892	blood:	n/a	n/a
45	E2F4	chr1:74776700-74776900	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:74791612-74791689	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:74759287-74759597	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:74701224-74701434	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:74680614-74680637	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr1:74782034-74782339	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74719316-74719366	HRE	kidney:	n/a
2	chr1:74719316-74719366	AG09319	gingival:	n/a
3	chr1:74719316-74719366	GM12892	blood:	n/a
4	chr1:74719316-74719366	AG04449	skin:	fetal
5	chr1:74719316-74719366	HCF	heart:	n/a
6	chr1:74719316-74719366	H1-hESC	embryonic stem cell:	embryo
7	chr1:74719316-74719366	GM06990	blood:	n/a
8	chr1:74719316-74719366	GM19239	blood:	n/a
9	chr1:74719316-74719366	IMR90	lung:	fetal
10	chr1:74719316-74719366	HepG2	liver:	n/a
11	chr1:74719316-74719366	NHDF-neo	bronchial:	n/a
12	chr1:74719316-74719366	HRCEpiC	kidney:	n/a
13	chr1:74719316-74719366	HCT-116	colon:	n/a
14	chr1:74719316-74719366	PFSK-1	brain:	n/a
15	chr1:74719316-74719366	HL-60	blood:	n/a
16	chr1:74719316-74719366	MCF10A-Er-Src	breast:	n/a
17	chr1:74719316-74719366	RPTEC	kidney:	n/a
18	chr1:74719316-74719366	CMK	blood:	n/a
19	chr1:74719316-74719366	HRPEpiC	eye:	n/a
20	chr1:74719316-74719366	HCM	heart:	n/a
21	chr1:74719316-74719366	BE2_C	brain:	n/a
22	chr1:74719316-74719366	SK-N-MC	brain:	n/a
23	chr1:74719316-74719366	ProgFib	skin:	n/a
24	chr1:74719316-74719366	Hela-S3	cervix:	n/a
25	chr1:74719316-74719366	SK-N-SH	brain:	n/a
26	chr1:74719316-74719366	NT2-D1	testis:	n/a
27	chr1:74719316-74719366	HUVEC	blood vessel:	n/a
28	chr1:74719316-74719366	HNPCEpiC	eye:	n/a
29	chr1:74719316-74719366	A549	lung:	n/a
30	chr1:74719316-74719366	K562	blood:	n/a
31	chr1:74719316-74719366	AG10803	skin:	n/a
32	chr1:74719316-74719366	T-47D	breast:	n/a
33	chr1:74719316-74719366	BJ	skin:	n/a
34	chr1:74719316-74719366	LNCaP	prostate:	n/a
35	chr1:74719316-74719366	GM12891	blood:	n/a
36	chr1:74719316-74719366	HEK293	kidney:	embryo
37	chr1:74719316-74719366	NB4	blood:	n/a
38	chr1:74719316-74719366	PrEC	prostate:	n/a
39	chr1:74719316-74719366	AG04450	lung:	fetal
40	chr1:74719316-74719366	MCF-7	breast:	n/a
41	chr1:74719316-74719366	AoSMC	blood vessel:	n/a
42	chr1:74719316-74719366	NHBE	bronchial:	n/a
43	chr1:74719316-74719366	PANC-1	pancreas:	n/a
44	chr1:74719316-74719366	ECC-1	luminal epithelium:	n/a
45	chr1:74719316-74719366	NH-A	brain:	n/a
46	chr1:74719316-74719366	Jurkat	blood:	n/a
47	chr1:74719316-74719366	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:74719316-74719366	HIPEpiC	eye:	n/a
49	chr1:74719316-74719366	HEEpiC	esophagus:	n/a
50	chr1:74719316-74719366	Caco-2	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
2	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
3	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
4	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
5	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
6	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
7	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
8	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
9	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
10	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
11	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
12	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
13	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
14	chr1:74662396..74665247-chr1:74681410..74684026,2	K562	blood:
15	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
16	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
17	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:

No data

Variant related genes	Relation type
TNNI3K	TF binding region
TNNI3K	CpG island
ENSG00000259030	chromatin interactions
ENSG00000254685	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000162620	chromatin interactions

Extended variants
information (count: 4643 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4643 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs485929	chr1:74678285-74678286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550539617	chr1:74678304-74678305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182547384	chr1:74678383-74678384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537251364	chr1:74678389-74678390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186462495	chr1:74678412-74678413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115184775	chr1:74678515-74678516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191107430	chr1:74678550-74678551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs488813	chr1:74678604-74678605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs577976677	chr1:74678608-74678609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202129715	chr1:74678624-74678625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs67512020	chr1:74678625-74678626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374981235	chr1:74678629-74678630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545329897	chr1:74678633-74678634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183712498	chr1:74678641-74678642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189200784	chr1:74678699-74678700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72964104	chr1:74678744-74678745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561491978	chr1:74678763-74678764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117023704	chr1:74678807-74678808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192865457	chr1:74678809-74678810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536766164	chr1:74678824-74678825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559048557	chr1:74678833-74678834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532946576	chr1:74678863-74678864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371596806	chr1:74678873-74678874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs477134	chr1:74678914-74678915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs569926131	chr1:74678925-74678926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530747742	chr1:74678950-74678951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548746505	chr1:74679012-74679013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569762720	chr1:74679019-74679020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368878053	chr1:74679081-74679082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547067524	chr1:74679083-74679084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116245877	chr1:74679091-74679092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534761174	chr1:74679097-74679098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553051819	chr1:74679124-74679125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571695220	chr1:74679149-74679150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77330641	chr1:74679192-74679193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557110672	chr1:74679194-74679195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376588838	chr1:74679204-74679205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373408387	chr1:74679219-74679220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs67800484	chr1:74679220-74679221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75342313	chr1:74679230-74679231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79769782	chr1:74679231-74679232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543362914	chr1:74679266-74679267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111516850	chr1:74679272-74679273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184720341	chr1:74679287-74679288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573488459	chr1:74679326-74679327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541082213	chr1:74679331-74679332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537038611	chr1:74679364-74679365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558483260	chr1:74679377-74679378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372521704	chr1:74679385-74679386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559397998	chr1:74679386-74679387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74664800-74680400	Weak transcription	Fetal Brain Female	brain
2	chr1:74664800-74688200	Weak transcription	Psoas Muscle	Psoas
3	chr1:74665000-74690200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr1:74665600-74680000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr1:74665600-74689200	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:74671200-74679800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:74671200-74694800	Weak transcription	Left Ventricle	heart
8	chr1:74671400-74678400	Weak transcription	Brain Substantia Nigra	brain
9	chr1:74671400-74683000	Weak transcription	Adipose Nuclei	Adipose
10	chr1:74671400-74719400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr1:74671400-74751800	Weak transcription	Ovary	ovary
12	chr1:74672600-74678400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:74672600-74688000	Weak transcription	Liver	Liver
14	chr1:74675800-74724000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr1:74676000-74680600	Weak transcription	Fetal Brain Male	brain
16	chr1:74678400-74678600	Enhancers	Brain Substantia Nigra	brain
17	chr1:74679400-74680800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:74680000-74680200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:74680000-74682800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:74680200-74680400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:74680400-74680600	Enhancers	Fetal Brain Female	brain
22	chr1:74680600-74681200	Weak transcription	Fetal Brain Female	brain
23	chr1:74680600-74681400	Enhancers	Fetal Brain Male	brain
24	chr1:74680800-74681800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:74681200-74682000	Enhancers	Fetal Brain Female	brain
26	chr1:74681200-74682200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:74681400-74684000	Weak transcription	Fetal Brain Male	brain
28	chr1:74681800-74682000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:74684000-74684400	Enhancers	Fetal Brain Male	brain
30	chr1:74686400-74687800	Weak transcription	Adipose Nuclei	Adipose
31	chr1:74686600-74689400	Enhancers	Stomach Mucosa	stomach
32	chr1:74686800-74687000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:74687200-74687600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:74688000-74688600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:74688200-74688400	Enhancers	A549	lung
36	chr1:74697800-74710600	Weak transcription	Psoas Muscle	Psoas
37	chr1:74699000-74700800	Enhancers	Fetal Heart	heart
38	chr1:74699200-74699600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:74700600-74713800	Weak transcription	Adipose Nuclei	Adipose
40	chr1:74700800-74701000	Flanking Active TSS	Fetal Heart	heart
41	chr1:74701000-74703400	Active TSS	Fetal Heart	heart
42	chr1:74701600-74704200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:74701600-74704200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:74701800-74705000	Active TSS	Right Atrium	heart
45	chr1:74702000-74702400	Active TSS	Right Ventricle	heart
46	chr1:74702200-74702600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:74702200-74703800	Active TSS	Left Ventricle	heart
48	chr1:74702400-74703200	Weak transcription	Right Ventricle	heart
49	chr1:74703200-74703800	Active TSS	Right Ventricle	heart
50	chr1:74703400-74703600	Transcr. at gene 5' and 3'	Fetal Heart	heart

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