Variant report

Variant	nsv1003386
Chromosome Location	chr1:77305197-77375536
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:694)
CpG islands
(count:1223)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:77366970-77367170	HepG2	liver:	n/a	n/a
2	ATF1	chr1:77335771-77336079	K562	blood:	n/a	n/a
3	ATF1	chr1:77318303-77318453	K562	blood:	n/a	n/a
4	ATF2	chr1:77337114-77337654	GM12878	blood:	n/a	n/a
5	BACH1	chr1:77333208-77333337	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:77337236-77337654	GM12878	blood:	n/a	n/a
7	BATF	chr1:77337272-77337608	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:77367001-77367193	K562	blood:	n/a	n/a
9	BHLHE40	chr1:77337170-77337568	GM12878	blood:	n/a	n/a
10	CBX3	chr1:77366821-77367350	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:77314766-77315027	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:77314903-77314952	K562	blood:	n/a	n/a
13	CEBPB	chr1:77338373-77338595	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:77333624-77334049	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:77338534-77338691	A549	lung:	n/a	n/a
16	CEBPB	chr1:77357653-77358035	IMR90	lung:	n/a	chr1:77357850-77357863 chr1:77357994-77358007
17	CEBPB	chr1:77314870-77315040	A549	lung:	n/a	n/a
18	CHD1	chr1:77333558-77334048	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr1:77366743-77367219	IMR90	lung:	n/a	n/a
20	CHD1	chr1:77334553-77334859	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr1:77337410-77337701	GM12878	blood:	n/a	n/a
22	CHD2	chr1:77333683-77334121	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:77332918-77333425	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr1:77332973-77335016	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:77366960-77367110	AG04449	skin:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
26	CTCF	chr1:77366935-77367151	MCF-7	breast:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
27	CTCF	chr1:77333060-77333210	HA-sp	spinal cord:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
28	CTCF	chr1:77366960-77367110	GM12870	blood:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
29	CTCF	chr1:77333040-77333190	HBMEC	blood vessel:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
30	CTCF	chr1:77367020-77367170	WI-38	lung:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
31	CTCF	chr1:77333900-77334050	HRE	kidney:	n/a	n/a
32	CTCF	chr1:77334100-77334250	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr1:77366940-77367090	AG04449	skin:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
34	CTCF	chr1:77333700-77333850	NHEK	skin:	n/a	n/a
35	CTCF	chr1:77334177-77334215	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:77333796-77334143	GM12878	blood:	n/a	n/a
37	CTCF	chr1:77366931-77367170	Pancreas_OC	pancreas:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
38	CTCF	chr1:77366936-77367148	MCF-7	breast:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
39	CTCF	chr1:77366940-77367090	HCT-116	colon:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
40	CTCF	chr1:77366892-77367187	GM12878	blood:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
41	CTCF	chr1:77366940-77367090	K562	blood:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
42	CTCF	chr1:77366880-77367030	WI-38	lung:	n/a	n/a
43	CTCF	chr1:77366580-77366730	AG09319	gingival:	n/a	chr1:77366665-77366686
44	CTCF	chr1:77366980-77367130	RPTEC	kidney:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
45	CTCF	chr1:77333020-77333170	HEK293	kidney:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
46	CTCF	chr1:77366960-77367110	HPF	lung:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
47	CTCF	chr1:77366960-77367110	HVMF	connective:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
48	CTCF	chr1:77366654-77367238	IMR90	lung:	n/a	chr1:77366665-77366686 chr1:77367032-77367053 chr1:77367030-77367048
49	CTCF	chr1:77366920-77367070	Caco-2	colon:	n/a	chr1:77367032-77367053 chr1:77367030-77367048
50	CTCF	chr1:77333840-77333990	NHDF-neo	bronchial:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77333138-77333188	HEEpiC	esophagus:	n/a
2	chr1:77333122-77333172	GM12878	blood:	n/a
3	chr1:77332993-77333043	ovcar-3	ovarian:	n/a
4	chr1:77333138-77333188	HEEpiC	esophagus:	n/a
5	chr1:77333122-77333172	GM12878	blood:	n/a
6	chr1:77332993-77333043	ovcar-3	ovarian:	n/a
7	chr1:77333074-77333124	HUVEC	blood vessel:	n/a
8	chr1:77334748-77334798	NHDF-neo	bronchial:	n/a
9	chr1:77333159-77333209	BE2_C	brain:	n/a
10	chr1:77333074-77333124	Jurkat	blood:	n/a
11	chr1:77333138-77333188	IMR90	lung:	fetal
12	chr1:77334177-77334227	BJ	skin:	n/a
13	chr1:77331940-77331990	SAEC	small airway:	n/a
14	chr1:77333122-77333172	HL-60	blood:	n/a
15	chr1:77331940-77331990	HepG2	liver:	n/a
16	chr1:77333159-77333209	SAEC	small airway:	n/a
17	chr1:77332993-77333043	SK-N-SH_RA	brain:	n/a
18	chr1:77334070-77334120	HRE	kidney:	n/a
19	chr1:77334678-77334728	RPTEC	kidney:	n/a
20	chr1:77334070-77334120	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:77333138-77333188	AG04450	lung:	fetal
22	chr1:77307268-77307318	AoSMC	blood vessel:	n/a
23	chr1:77334070-77334120	AG09309	skin:	n/a
24	chr1:77334207-77334257	RPTEC	kidney:	n/a
25	chr1:77334177-77334227	GM12892	blood:	n/a
26	chr1:77333860-77333910	MCF-7	breast:	n/a
27	chr1:77333198-77333248	HNPCEpiC	eye:	n/a
28	chr1:77333198-77333248	AG10803	skin:	n/a
29	chr1:77334256-77334306	HCPEpiC	choroid plexus:	n/a
30	chr1:77333074-77333124	HCT-116	colon:	n/a
31	chr1:77322109-77322159	Caco-2	colon:	n/a
32	chr1:77333074-77333124	AG09319	gingival:	n/a
33	chr1:77332991-77333041	LNCaP	prostate:	n/a
34	chr1:77333074-77333124	Caco-2	colon:	n/a
35	chr1:77333860-77333910	HCT-116	colon:	n/a
36	chr1:77322109-77322159	H1-hESC	embryonic stem cell:	embryo
37	chr1:77333860-77333910	SK-N-SH	brain:	n/a
38	chr1:77334045-77334095	HUVEC	blood vessel:	n/a
39	chr1:77332991-77333041	NB4	blood:	n/a
40	chr1:77333860-77333910	GM12891	blood:	n/a
41	chr1:77333074-77333124	AG09309	skin:	n/a
42	chr1:77334678-77334728	HCM	heart:	n/a
43	chr1:77332993-77333043	SAEC	small airway:	n/a
44	chr1:77333122-77333172	H1-hESC	embryonic stem cell:	embryo
45	chr1:77333159-77333209	HCPEpiC	choroid plexus:	n/a
46	chr1:77322109-77322159	T-47D	breast:	n/a
47	chr1:77331940-77331990	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:77332991-77333041	ECC-1	luminal epithelium:	n/a
49	chr1:77333198-77333248	PANC-1	pancreas:	n/a
50	chr1:77333198-77333248	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:77366245..77367518-chr1:77591630..77592525,3	K562	blood:
2	chr1:77325804..77328743-chr1:77329882..77332282,4	K562	blood:
3	chr1:77335357..77338179-chr1:77371008..77373403,2	K562	blood:
4	chr1:77319935..77321770-chr1:77325781..77328772,2	K562	blood:
5	chr1:77366800..77367486-chr1:77496947..77497587,3	MCF-7	breast:
6	chr1:76796406..76797312-chr1:77366615..77367452,3	MCF-7	breast:
7	chr1:77371424..77372095-chr2:11259981..11260798,2	MCF-7	breast:
8	chr1:77335357..77338179-chr1:77371008..77373403,2	K562	blood:
9	chr1:77319935..77321770-chr1:77325781..77328772,2	K562	blood:
10	chr1:77325804..77328743-chr1:77329882..77332282,4	K562	blood:
11	chr1:77374791..77376785-chr17:38477195..38479729,2	MCF-7	breast:
12	chr1:77366569..77367440-chr1:77591672..77592573,4	MCF-7	breast:
13	chr1:77326930..77328743-chr1:77330284..77333050,4	K562	blood:
14	chr1:77326930..77328743-chr1:77330284..77333050,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST6GALNAC5-2	chr1:77307009-77307116	NONHSAT004016
2	lnc-ST6GALNAC5-2	chr1:77306357-77306520	NONHSAT004016
3	lnc-ST6GALNAC5-2	chr1:77306193-77306274	NONHSAT004016
4	lnc-ST6GALNAC5-2	chr1:77316613-77316755	NONHSAT004016

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ST6GALNAC5	hsa-miR-148b-3p	chr1:77334423-77334427

Variant related genes	Relation type
ST6GALNAC5	TF binding region
ST6GALNAC5	CpG island
ENSG00000131759	chromatin interactions

Extended variants
information (count: 2259 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533121210	chr1:77305237-77305238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373380773	chr1:77305240-77305241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377022266	chr1:77305244-77305245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536339824	chr1:77305264-77305265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554679233	chr1:77305265-77305266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572950569	chr1:77305296-77305297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192229541	chr1:77305314-77305315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56289609	chr1:77305319-77305320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371565185	chr1:77305329-77305330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372502671	chr1:77305355-77305356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376487078	chr1:77305399-77305400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371823362	chr1:77305401-77305402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374581528	chr1:77305403-77305404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4998665	chr1:77305415-77305416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375345650	chr1:77305417-77305418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9726328	chr1:77305423-77305424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533126339	chr1:77305431-77305432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58158012	chr1:77305432-77305433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9726020	chr1:77305433-77305434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544973815	chr1:77305456-77305457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183566309	chr1:77305492-77305493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149671029	chr1:77305534-77305535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542732296	chr1:77305540-77305541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528307394	chr1:77305570-77305571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561476759	chr1:77305607-77305608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377004175	chr1:77305659-77305660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114655559	chr1:77305791-77305792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187860738	chr1:77305800-77305801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565552482	chr1:77305845-77305846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532874710	chr1:77305878-77305879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9726362	chr1:77305885-77305886	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs568849911	chr1:77305894-77305895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145452974	chr1:77305915-77305916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78818207	chr1:77305934-77305935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566572163	chr1:77305969-77305970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs57691753	chr1:77305979-77305980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs529253466	chr1:77306007-77306008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549521275	chr1:77306017-77306018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546748749	chr1:77306057-77306058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376524639	chr1:77306059-77306060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558738943	chr1:77306067-77306068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192385241	chr1:77306073-77306074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113485065	chr1:77306127-77306128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112919532	chr1:77306134-77306135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111687577	chr1:77306141-77306142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142684859	chr1:77306149-77306150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147624973	chr1:77306159-77306160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184546974	chr1:77306176-77306177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561181921	chr1:77306178-77306179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142180471	chr1:77306252-77306253	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77303200-77307400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:77305800-77306600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:77306200-77308000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:77306600-77307600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:77306800-77307600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:77307000-77307600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:77307000-77308000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:77307000-77308000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:77307200-77308000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:77307400-77307800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr1:77307400-77308000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:77309000-77309600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr1:77309400-77309600	Enhancers	GM12878-XiMat	blood
14	chr1:77309400-77309800	Enhancers	Primary T cells fromperipheralblood	blood
15	chr1:77309600-77309800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr1:77309600-77310000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:77309600-77310000	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr1:77309600-77310200	Active TSS	GM12878-XiMat	blood
19	chr1:77309600-77310200	Active TSS	Hela-S3	cervix
20	chr1:77309600-77310400	Enhancers	Primary T cells from cord blood	blood
21	chr1:77309600-77310400	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr1:77309600-77310600	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr1:77309800-77310200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
24	chr1:77309800-77310400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:77310000-77310400	Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr1:77310000-77310600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr1:77311000-77311600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:77311400-77311800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:77314800-77315200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:77319000-77319600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:77319000-77319800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr1:77319000-77320400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:77319200-77319800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr1:77319400-77319600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:77319400-77319800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:77319400-77319800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:77319400-77320400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr1:77319600-77320200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr1:77319600-77320200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:77319600-77320600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:77319800-77320000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr1:77319800-77320000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr1:77319800-77320000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr1:77319800-77320400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr1:77319800-77321800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr1:77319800-77333200	Weak transcription	Gastric	stomach
47	chr1:77320000-77320200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:77320000-77320200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:77320000-77320200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:77320000-77320400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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