Variant report

Variant	nsv1010903
Chromosome Location	chr1:104483363-105468941
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2485)
CpG islands
(count:611)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104905681-104905751	K562	blood:	n/a	n/a
2	ARID3A	chr1:105190891-105191002	K562	blood:	n/a	n/a
3	ARID3A	chr1:105190829-105191091	HepG2	liver:	n/a	n/a
4	ATF1	chr1:105342024-105342172	K562	blood:	n/a	n/a
5	ATF1	chr1:104810879-104811002	K562	blood:	n/a	n/a
6	ATF1	chr1:105249550-105249744	K562	blood:	n/a	n/a
7	ATF2	chr1:105302672-105303078	GM12878	blood:	n/a	n/a
8	ATF2	chr1:105302490-105303131	GM12878	blood:	n/a	n/a
9	BACH1	chr1:104782197-104782240	K562	blood:	n/a	n/a
10	BACH1	chr1:104807443-104807472	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:105263394-105263707	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:104818992-104819156	K562	blood:	n/a	n/a
13	BACH1	chr1:104612948-104613054	K562	blood:	n/a	n/a
14	BACH1	chr1:104812358-104812719	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:104833850-104834086	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:105117291-105117491	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:105340677-105340678	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:105010231-105010532	GM12878	blood:	n/a	chr1:105010343-105010354
19	BATF	chr1:105249568-105249877	GM12878	blood:	n/a	n/a
20	BATF	chr1:105249516-105249842	GM12878	blood:	n/a	n/a
21	BATF	chr1:105302654-105302979	GM12878	blood:	n/a	n/a
22	BATF	chr1:105010189-105010541	GM12878	blood:	n/a	chr1:105010343-105010354
23	BATF	chr1:104930806-104931053	GM12878	blood:	n/a	n/a
24	BATF	chr1:105302655-105302965	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:105307818-105308035	GM12878	blood:	n/a	chr1:105307996-105308004
26	BCL11A	chr1:105249605-105249760	GM12878	blood:	n/a	chr1:105249692-105249701
27	BCL11A	chr1:104635351-104635616	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr1:105302706-105302970	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:105249581-105249831	GM12878	blood:	n/a	chr1:105249754-105249763 chr1:105249692-105249701
30	BCL3	chr1:104751628-104751863	GM12878	blood:	n/a	n/a
31	BCL3	chr1:104751571-104751823	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:105302522-105303109	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:105135589-105135971	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:104865956-104865961	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:105311116-105311444	GM12878	blood:	n/a	n/a
36	BRCA1	chr1:105323229-105323372	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr1:104519193-104519299	GM12878	blood:	n/a	n/a
38	BRCA1	chr1:104524798-104524808	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:105008729-105009077	A549	lung:	n/a	n/a
40	CEBPB	chr1:105250603-105250905	HepG2	liver:	n/a	chr1:105250755-105250766 chr1:105250726-105250737
41	CEBPB	chr1:105010861-105011166	HepG2	liver:	n/a	chr1:105011000-105011011
42	CEBPB	chr1:104500309-104500557	HepG2	liver:	n/a	chr1:104500435-104500444 chr1:104500433-104500446 chr1:104500435-104500444 chr1:104500433-104500444 chr1:104500435-104500444 chr1:104500433-104500444 chr1:104500433-104500446 chr1:104500435-104500444 chr1:104500434-104500445
43	CEBPB	chr1:105043292-105043470	K562	blood:	n/a	n/a
44	CEBPB	chr1:105068176-105068466	HepG2	liver:	n/a	chr1:105068339-105068352 chr1:105068287-105068300 chr1:105068340-105068351
45	CEBPB	chr1:104663974-104664248	A549	lung:	n/a	chr1:104664078-104664091 chr1:104664079-104664090 chr1:104664080-104664089 chr1:104664078-104664091 chr1:104664078-104664089
46	CEBPB	chr1:105035577-105035609	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:104528434-104528672	HepG2	liver:	n/a	chr1:104528542-104528553 chr1:104528450-104528461 chr1:104528541-104528554
48	CEBPB	chr1:104992286-104992590	IMR90	lung:	n/a	chr1:104992449-104992460 chr1:104992299-104992311
49	CEBPB	chr1:104753894-104754116	K562	blood:	n/a	chr1:104753931-104753942
50	CEBPB	chr1:105068906-105069306	HepG2	liver:	n/a	chr1:105069114-105069125 chr1:105068916-105068927 chr1:105069113-105069124 chr1:105069154-105069165 chr1:105069113-105069126 chr1:105069113-105069124

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104696931-104696981	BE2_C	brain:	n/a
2	chr1:104696931-104696981	BE2_C	brain:	n/a
3	chr1:104615867-104615917	HCPEpiC	choroid plexus:	n/a
4	chr1:105318962-105319012	U87	brain:	n/a
5	chr1:104616267-104616317	AG10803	skin:	n/a
6	chr1:105207165-105207215	HCT-116	colon:	n/a
7	chr1:104616267-104616317	RPTEC	kidney:	n/a
8	chr1:105207165-105207215	NHDF-neo	bronchial:	n/a
9	chr1:104615609-104615659	AG09319	gingival:	n/a
10	chr1:104616267-104616317	HAEpiC	amniotic membrane:	n/a
11	chr1:105031120-105031170	PFSK-1	brain:	n/a
12	chr1:104616118-104616168	GM12892	blood:	n/a
13	chr1:104635600-104635650	AG04450	lung:	fetal
14	chr1:105318962-105319012	AG10803	skin:	n/a
15	chr1:105031120-105031170	HEEpiC	esophagus:	n/a
16	chr1:105318962-105319012	ECC-1	luminal epithelium:	n/a
17	chr1:104615609-104615659	HRE	kidney:	n/a
18	chr1:104616118-104616168	SK-N-SH	brain:	n/a
19	chr1:104696931-104696981	HNPCEpiC	eye:	n/a
20	chr1:104616118-104616168	A549	lung:	n/a
21	chr1:105031120-105031170	HCT-116	colon:	n/a
22	chr1:104615867-104615917	HCM	heart:	n/a
23	chr1:104523359-104523409	PANC-1	pancreas:	n/a
24	chr1:104696931-104696981	ProgFib	skin:	n/a
25	chr1:105031120-105031170	SK-N-SH_RA	brain:	n/a
26	chr1:104615609-104615659	RPTEC	kidney:	n/a
27	chr1:105031120-105031170	U87	brain:	n/a
28	chr1:104616267-104616317	HRE	kidney:	n/a
29	chr1:104635600-104635650	SK-N-MC	brain:	n/a
30	chr1:104696931-104696981	AG10803	skin:	n/a
31	chr1:104616118-104616168	AoSMC	blood vessel:	n/a
32	chr1:104523359-104523409	ProgFib	skin:	n/a
33	chr1:104615867-104615917	SK-N-MC	brain:	n/a
34	chr1:104615867-104615917	GM12892	blood:	n/a
35	chr1:104615609-104615659	AoSMC	blood vessel:	n/a
36	chr1:104615867-104615917	Jurkat	blood:	n/a
37	chr1:104616267-104616317	NB4	blood:	n/a
38	chr1:104615867-104615917	GM19239	blood:	n/a
39	chr1:104635600-104635650	HCT-116	colon:	n/a
40	chr1:104615867-104615917	PANC-1	pancreas:	n/a
41	chr1:105207165-105207215	AoSMC	blood vessel:	n/a
42	chr1:105318962-105319012	SAEC	small airway:	n/a
43	chr1:104615609-104615659	GM19239	blood:	n/a
44	chr1:105031120-105031170	HRCEpiC	kidney:	n/a
45	chr1:105318962-105319012	GM19239	blood:	n/a
46	chr1:104615867-104615917	BE2_C	brain:	n/a
47	chr1:105207165-105207215	SK-N-MC	brain:	n/a
48	chr1:104615867-104615917	GM12878	blood:	n/a
49	chr1:104696931-104696981	ovcar-3	ovarian:	n/a
50	chr1:104616267-104616317	NHBE	bronchial:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:105016188..105019008-chr1:105023747..105026676,2	K562	blood:
2	chr1:105128438..105130994-chr1:105132786..105134781,2	K562	blood:
3	chr1:105322921..105323781-chr1:106335621..106336447,4	MCF-7	breast:
4	chr1:105059139..105061952-chr1:105062553..105064235,2	K562	blood:
5	chr1:105322701..105323694-chr1:106151023..106151974,2	MCF-7	breast:
6	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
7	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
8	chr1:105464233..105466305-chr1:105536432..105538277,2	MCF-7	breast:
9	chr1:105021052..105022674-chr1:105034468..105036725,2	K562	blood:
10	chr1:105016188..105019008-chr1:105023747..105026676,2	K562	blood:
11	chr1:105059139..105061952-chr1:105062553..105064235,2	K562	blood:
12	chr1:105225780..105228608-chr1:105234068..105236251,2	K562	blood:
13	chr1:104725861..104727973-chr1:104730004..104731951,2	K562	blood:
14	chr1:104659954..104662571-chr1:104673545..104675551,2	K562	blood:
15	chr1:105323182..105323702-chr1:106336107..106336743,2	K562	blood:
16	chr1:104693612..104696464-chr1:104700325..104702158,2	K562	blood:
17	chr1:104490807..104491700-chr1:104674682..104675320,2	MCF-7	breast:
18	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
19	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:
20	chr1:105128438..105130994-chr1:105132786..105134781,2	K562	blood:
21	chr1:105190498..105191127-chr1:106335842..106336840,2	MCF-7	breast:
22	chr1:104725861..104727973-chr1:104730004..104731951,2	K562	blood:
23	chr1:104490807..104491700-chr1:104674682..104675320,2	MCF-7	breast:
24	chr1:104659954..104662571-chr1:104673545..104675551,2	K562	blood:
25	chr1:105465225..105466908-chr1:105470582..105473577,2	K562	blood:
26	chr1:105021052..105022674-chr1:105034468..105036725,2	K562	blood:
27	chr1:105322783..105323719-chr1:106810790..106811327,2	MCF-7	breast:
28	chr1:105396022..105396528-chr2:15494186..15495100,2	MCF-7	breast:
29	chr1:105225780..105228608-chr1:105234068..105236251,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1C-2	chr1:104672444-104672483	XLOC_000326
2	lnc-AMY1C-2	chr1:104668179-104668541	XLOC_000326
3	lnc-AMY1C-2	chr1:104668178-104668541	NONHSAT004905
4	lnc-AMY1C-2	chr1:104672443-104672483	NONHSAT004905

No data

Variant related genes	Relation type
ENSG00000243500	TF binding region
ENSG00000215869	TF binding region
FTLP17	TF binding region
ENSG00000243500	CpG island
ENSG00000215869	CpG island
FTLP17	CpG island
ENSG00000228347	chromatin interactions

Extended variants
information (count: 9679 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:9679 , 50 per page) page: 1 2 3 4 5 6 7 ... 194

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555014680	chr1:104483810-104483811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs3849298	chr1:104483838-104483839	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541327982	chr1:104483839-104483840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529155553	chr1:104483895-104483896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543570130	chr1:104483897-104483898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4520426	chr1:104483941-104483942	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs578199371	chr1:104483973-104483974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7554165	chr1:104483975-104483976	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs188763102	chr1:104483987-104483988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200654797	chr1:104484004-104484005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530981206	chr1:104484042-104484043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192693049	chr1:104484069-104484070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561094012	chr1:104484084-104484085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116524396	chr1:104484089-104484090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7545401	chr1:104484099-104484100	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565684668	chr1:104484102-104484103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532953352	chr1:104484180-104484181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150137092	chr1:104484217-104484218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185035065	chr1:104484233-104484234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138569225	chr1:104484237-104484238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555454904	chr1:104484247-104484248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567136160	chr1:104484343-104484344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551284	chr1:104484407-104484408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs370776637	chr1:104484410-104484411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578259570	chr1:104484428-104484429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545723762	chr1:104484431-104484432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115718695	chr1:104484472-104484473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78691055	chr1:104484485-104484486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542742598	chr1:104484500-104484501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149330330	chr1:104484501-104484502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs662162	chr1:104484628-104484629	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548714	chr1:104484630-104484631	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564948551	chr1:104484634-104484635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61816494	chr1:104484650-104484651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530885562	chr1:104484665-104484666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372326781	chr1:104484666-104484667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77810808	chr1:104484680-104484681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11465131	chr1:104484681-104484682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79476985	chr1:104484682-104484683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75359743	chr1:104484683-104484684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144575450	chr1:104484713-104484714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530767135	chr1:104484775-104484776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548779630	chr1:104484783-104484784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567399415	chr1:104484834-104484835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534311428	chr1:104484846-104484847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546576938	chr1:104484919-104484920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7548445	chr1:104484934-104484935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539306799	chr1:104484947-104484948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7516686	chr1:104484953-104484954	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575888555	chr1:104484973-104484974	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	17550852	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104483800-104484800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:104483800-104485800	Enhancers	Fetal Lung	lung
3	chr1:104484000-104484400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:104484200-104485000	Enhancers	Pancreas	Pancrea
5	chr1:104485400-104486000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr1:104485800-104487400	Weak transcription	Fetal Lung	lung
7	chr1:104487400-104487600	Enhancers	Fetal Lung	lung
8	chr1:104488400-104488600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr1:104488600-104488800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:104492400-104493000	Enhancers	Fetal Brain Female	brain
11	chr1:104492400-104493000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr1:104502200-104503000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:104502200-104504000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:104503200-104504000	ZNF genes & repeats	Pancreas	Pancrea
15	chr1:104503600-104503800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:104503800-104504000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:104542800-104543400	Enhancers	Fetal Brain Female	brain
18	chr1:104566000-104566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:104570800-104571400	Active TSS	Fetal Lung	lung
20	chr1:104571400-104572200	Weak transcription	Fetal Lung	lung
21	chr1:104572200-104573600	Enhancers	Fetal Lung	lung
22	chr1:104573200-104573600	Enhancers	Fetal Heart	heart
23	chr1:104594600-104595000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:104595200-104599400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:104599200-104600800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr1:104599400-104600000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:104599400-104600000	Active TSS	HepG2	liver
28	chr1:104599400-104600400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr1:104599400-104600400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:104599400-104600400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:104599400-104600600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:104599400-104600800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:104599600-104600000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:104599600-104600600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:104599600-104600600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:104599600-104600600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:104599600-104600600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:104599600-104600600	Enhancers	Colonic Mucosa	Colon
39	chr1:104599600-104600800	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr1:104600000-104600400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr1:104600000-104600400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:104600200-104600600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:104615600-104616200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:104615600-104616400	Active TSS	Pancreas	Pancrea
45	chr1:104615600-104616400	Active TSS	Right Ventricle	heart
46	chr1:104615600-104616600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:104615600-104616600	Active TSS	Fetal Stomach	stomach
48	chr1:104626000-104627000	Enhancers	Fetal Heart	heart
49	chr1:104626200-104626600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:104626200-104626600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast

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