Variant report

Variant	nsv1002663
Chromosome Location	chr1:71372715-71465508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:475)
CpG islands
(count:62)
Chromatin interactive
region (count:26)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71460522-71460848	K562	blood:	n/a	n/a
2	ARID3A	chr1:71436198-71436440	K562	blood:	n/a	n/a
3	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
4	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
5	ATF1	chr1:71427045-71427515	K562	blood:	n/a	n/a
6	ATF1	chr1:71375175-71375423	K562	blood:	n/a	n/a
7	BACH1	chr1:71377587-71377854	K562	blood:	n/a	n/a
8	BHLHE40	chr1:71427278-71427427	K562	blood:	n/a	n/a
9	BHLHE40	chr1:71436134-71436325	K562	blood:	n/a	n/a
10	CCNT2	chr1:71375173-71375436	K562	blood:	n/a	n/a
11	CEBPB	chr1:71413585-71413825	A549	lung:	n/a	chr1:71413682-71413693 chr1:71413711-71413724
12	CEBPB	chr1:71458228-71458549	K562	blood:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
13	CEBPB	chr1:71410721-71410977	HepG2	liver:	n/a	chr1:71410833-71410844
14	CEBPB	chr1:71375018-71375229	A549	lung:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
15	CEBPB	chr1:71458240-71458524	HepG2	liver:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
16	CEBPB	chr1:71374995-71375217	HepG2	liver:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
17	CEBPB	chr1:71444470-71444536	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:71374950-71375457	K562	blood:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
19	CEBPB	chr1:71375115-71375469	K562	blood:	n/a	chr1:71375115-71375126 chr1:71375116-71375125
20	CEBPB	chr1:71422052-71422132	K562	blood:	n/a	chr1:71422081-71422092
21	CEBPB	chr1:71374999-71375276	IMR90	lung:	n/a	chr1:71375115-71375126 chr1:71375116-71375125 chr1:71375114-71375125
22	CEBPB	chr1:71423310-71423611	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:71413576-71413806	HepG2	liver:	n/a	chr1:71413682-71413693 chr1:71413711-71413724
24	CEBPB	chr1:71421987-71422201	HepG2	liver:	n/a	chr1:71422081-71422092
25	CEBPB	chr1:71423305-71423526	K562	blood:	n/a	n/a
26	CEBPD	chr1:71438637-71439063	K562	blood:	n/a	n/a
27	CREB1	chr1:71375681-71375975	GM12878	blood:	n/a	n/a
28	CTCF	chr1:71431820-71431970	K562	blood:	n/a	n/a
29	CTCF	chr1:71431840-71431990	RPTEC	kidney:	n/a	n/a
30	CTCF	chr1:71429180-71429330	GM12874	blood:	n/a	n/a
31	CTCF	chr1:71431820-71431970	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr1:71429180-71429330	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr1:71431800-71431950	GM12868	blood:	n/a	n/a
34	CTCF	chr1:71431780-71431930	AG04450	lung:	n/a	n/a
35	CTCF	chr1:71431820-71431970	GM12875	blood:	n/a	n/a
36	CTCF	chr1:71431820-71431970	GM12869	blood:	n/a	n/a
37	CTCF	chr1:71431787-71432004	K562	blood:	n/a	n/a
38	CTCF	chr1:71429200-71429350	GM12868	blood:	n/a	n/a
39	CTCF	chr1:71431820-71431970	GM12873	blood:	n/a	n/a
40	CTCF	chr1:71431800-71431950	HFF	foreskin:	n/a	n/a
41	CTCF	chr1:71432279-71432285	NHEK	skin:	n/a	n/a
42	CTCF	chr1:71429182-71429437	K562	blood:	n/a	n/a
43	CTCF	chr1:71431820-71431970	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:71431740-71431890	HCM	heart:	n/a	n/a
45	CTCF	chr1:71431803-71431973	GM13977	blood:	n/a	n/a
46	CTCF	chr1:71431660-71431810	HCT-116	colon:	n/a	n/a
47	CTCF	chr1:71375840-71375990	GM06990	blood:	n/a	n/a
48	CTCF	chr1:71431820-71431970	AG04450	lung:	n/a	n/a
49	CTCF	chr1:71429219-71429377	GM19238	blood:	n/a	n/a
50	CTCF	chr1:71436160-71436310	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71418388-71418438	LNCaP	prostate:	n/a
2	chr1:71418388-71418438	LNCaP	prostate:	n/a
3	chr1:71418388-71418438	NHDF-neo	bronchial:	n/a
4	chr1:71418388-71418438	NB4	blood:	n/a
5	chr1:71418388-71418438	HAEpiC	amniotic membrane:	n/a
6	chr1:71418388-71418438	PFSK-1	brain:	n/a
7	chr1:71418388-71418438	SK-N-MC	brain:	n/a
8	chr1:71418388-71418438	HL-60	blood:	n/a
9	chr1:71418388-71418438	HepG2	liver:	n/a
10	chr1:71418388-71418438	AG04449	skin:	fetal
11	chr1:71418388-71418438	MCF-7	breast:	n/a
12	chr1:71418388-71418438	HEK293	kidney:	embryo
13	chr1:71418388-71418438	BJ	skin:	n/a
14	chr1:71418388-71418438	SAEC	small airway:	n/a
15	chr1:71418388-71418438	PrEC	prostate:	n/a
16	chr1:71418388-71418438	A549	lung:	n/a
17	chr1:71418388-71418438	GM06990	blood:	n/a
18	chr1:71418388-71418438	Hela-S3	cervix:	n/a
19	chr1:71418388-71418438	AG09309	skin:	n/a
20	chr1:71418388-71418438	HRCEpiC	kidney:	n/a
21	chr1:71418388-71418438	HCF	heart:	n/a
22	chr1:71418388-71418438	Caco-2	colon:	n/a
23	chr1:71418388-71418438	HRPEpiC	eye:	n/a
24	chr1:71418388-71418438	HCPEpiC	choroid plexus:	n/a
25	chr1:71418388-71418438	AoSMC	blood vessel:	n/a
26	chr1:71418388-71418438	IMR90	lung:	fetal
27	chr1:71418388-71418438	T-47D	breast:	n/a
28	chr1:71418388-71418438	AG09319	gingival:	n/a
29	chr1:71418388-71418438	HIPEpiC	eye:	n/a
30	chr1:71418388-71418438	K562	blood:	n/a
31	chr1:71418388-71418438	HMEC	breast:	n/a
32	chr1:71418388-71418438	HNPCEpiC	eye:	n/a
33	chr1:71418388-71418438	BE2_C	brain:	n/a
34	chr1:71418388-71418438	MCF10A-Er-Src	breast:	n/a
35	chr1:71418388-71418438	ProgFib	skin:	n/a
36	chr1:71418388-71418438	Hepatocyte	liver:	n/a
37	chr1:71418388-71418438	ovcar-3	ovarian:	n/a
38	chr1:71418388-71418438	NT2-D1	testis:	n/a
39	chr1:71418388-71418438	GM19239	blood:	n/a
40	chr1:71418388-71418438	AG10803	skin:	n/a
41	chr1:71418388-71418438	SK-N-SH_RA	brain:	n/a
42	chr1:71418388-71418438	GM12878	blood:	n/a
43	chr1:71418388-71418438	U87	brain:	n/a
44	chr1:71418388-71418438	HEEpiC	esophagus:	n/a
45	chr1:71418388-71418438	HUVEC	blood vessel:	n/a
46	chr1:71418388-71418438	GM12892	blood:	n/a
47	chr1:71418388-71418438	SK-N-SH	brain:	n/a
48	chr1:71418388-71418438	Jurkat	blood:	n/a
49	chr1:71418388-71418438	NH-A	brain:	n/a
50	chr1:71418388-71418438	RPTEC	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
2	chr1:71411854..71414751-chr1:71416719..71419463,2	K562	blood:
3	chr1:71374929..71377417-chr1:71518030..71520956,2	K562	blood:
4	chr1:71378991..71380997-chr1:71383679..71385899,2	K562	blood:
5	chr1:71348952..71350575-chr1:71372335..71374257,2	K562	blood:
6	chr1:71372779..71374433-chr1:71377421..71380381,2	K562	blood:
7	chr1:71398892..71400673-chr1:71400772..71403313,2	K562	blood:
8	chr1:71381219..71383532-chr1:71401301..71402871,2	K562	blood:
9	chr1:71373472..71375942-chr1:71510520..71512137,2	K562	blood:
10	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
11	chr1:70975940..70976451-chr1:71428828..71429462,2	MCF-7	breast:
12	chr1:71381219..71383532-chr1:71401301..71402871,2	K562	blood:
13	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
14	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
15	chr1:71150765..71151639-chr1:71429287..71429792,2	MCF-7	breast:
16	chr1:71389776..71391612-chr1:71519550..71521085,2	K562	blood:
17	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
18	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
19	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
20	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
21	chr1:71402954..71404643-chr1:71411844..71413632,2	K562	blood:
22	chr1:71427617..71429337-chr1:71437684..71440303,2	K562	blood:
23	chr1:71378991..71380997-chr1:71383679..71385899,2	K562	blood:
24	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
25	chr1:71372779..71374433-chr1:71377421..71380381,2	K562	blood:
26	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-3	chr1:71416584-71417176	ENSG00000235782.1
2	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
3	lnc-CTH-3	chr1:71416418-71416476	ENSG00000235782.1
4	lnc-CTH-12	chr1:71430529-71431707	NONHSAT003873
5	lnc-CTH-12	chr1:71426588-71426941	NONHSAT003873
6	lnc-CTH-3	chr1:71413062-71413158	ENSG00000235782.1

No data

Variant related genes	Relation type
ENSG00000235782	TF binding region
ENSG00000235782	CpG island
ENSG00000235782	chromatin interactions

Extended variants
information (count: 3275 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3275 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555227588	chr1:71372760-71372761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559617263	chr1:71372766-71372767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537537505	chr1:71372849-71372850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557528714	chr1:71372880-71372881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577289947	chr1:71372888-71372889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs59834528	chr1:71372915-71372916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201171267	chr1:71372931-71372932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374778077	chr1:71372936-71372937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546194323	chr1:71372960-71372961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143738810	chr1:71373014-71373015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187188014	chr1:71373037-71373038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146814275	chr1:71373082-71373083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140565773	chr1:71373118-71373119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190624554	chr1:71373119-71373120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543886511	chr1:71373194-71373195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150031569	chr1:71373198-71373199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532885394	chr1:71373242-71373243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528736469	chr1:71373247-71373248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546244164	chr1:71373250-71373251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145308501	chr1:71373267-71373268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116575096	chr1:71373282-71373283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114301931	chr1:71373321-71373322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181034575	chr1:71373328-71373329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116447556	chr1:71373347-71373348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376307809	chr1:71373348-71373349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558008193	chr1:71373361-71373362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548692809	chr1:71373396-71373397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570926450	chr1:71373475-71373476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539933952	chr1:71373535-71373536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74089133	chr1:71373546-71373547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs149223460	chr1:71373593-71373594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370082229	chr1:71373609-71373610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555676117	chr1:71373610-71373611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17541646	chr1:71373645-71373646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs544370776	chr1:71373664-71373665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146875680	chr1:71373684-71373685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377282633	chr1:71373685-71373686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532822403	chr1:71373691-71373692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147564163	chr1:71373708-71373709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs875727	chr1:71373738-71373739	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs115821531	chr1:71373742-71373743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548990081	chr1:71373787-71373788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs61777100	chr1:71373807-71373808	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185999424	chr1:71373828-71373829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551564640	chr1:71373859-71373860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141953060	chr1:71373865-71373866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570171284	chr1:71373866-71373867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539548859	chr1:71373871-71373872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553474066	chr1:71373873-71373874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566738684	chr1:71373878-71373879	Enhancers	n/a	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
small cell lung cancer	20016488	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
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71372200-71373400	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr1:71372200-71376400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:71372400-71376000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:71372400-71376200	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:71372400-71376200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:71372600-71373800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:71372800-71373200	Enhancers	Primary T cells from cord blood	blood
8	chr1:71372800-71377200	Enhancers	Dnd41	blood
9	chr1:71373200-71373600	Weak transcription	Primary T cells from cord blood	blood
10	chr1:71373200-71374800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:71373600-71376600	Enhancers	Primary T cells from cord blood	blood
12	chr1:71374000-71375200	Enhancers	Fetal Thymus	thymus
13	chr1:71374600-71376200	Enhancers	K562	blood
14	chr1:71374800-71376000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:71375200-71375600	Weak transcription	Fetal Thymus	thymus
16	chr1:71375600-71376600	Enhancers	Fetal Thymus	thymus
17	chr1:71376000-71376600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:71376200-71376600	Weak transcription	K562	blood
19	chr1:71376600-71377400	Enhancers	K562	blood
20	chr1:71377200-71380400	Weak transcription	Dnd41	blood
21	chr1:71377400-71381200	Weak transcription	K562	blood
22	chr1:71380400-71380800	Enhancers	Fetal Heart	heart
23	chr1:71380400-71382200	Enhancers	Adipose Nuclei	Adipose
24	chr1:71380400-71383400	Enhancers	Dnd41	blood
25	chr1:71380600-71380800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:71380600-71381200	Enhancers	Brain Germinal Matrix	brain
27	chr1:71380600-71381600	Enhancers	Rectal Smooth Muscle	rectum
28	chr1:71380800-71381400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:71380800-71381400	Enhancers	Colon Smooth Muscle	Colon
30	chr1:71381200-71381400	Enhancers	K562	blood
31	chr1:71381400-71382200	Weak transcription	K562	blood
32	chr1:71381400-71382600	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:71381400-71383000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:71382200-71382400	Enhancers	K562	blood
35	chr1:71382800-71383000	Enhancers	Colon Smooth Muscle	Colon
36	chr1:71383000-71386400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:71388000-71389400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:71394200-71394400	Enhancers	Pancreas	Pancrea
39	chr1:71394400-71397200	Weak transcription	Pancreas	Pancrea
40	chr1:71394600-71395200	Enhancers	Dnd41	blood
41	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:71394800-71396000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:71395200-71395400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr1:71395200-71395600	Weak transcription	Dnd41	blood
46	chr1:71395600-71396200	Enhancers	Adipose Nuclei	Adipose
47	chr1:71395600-71396200	Enhancers	Dnd41	blood
48	chr1:71395800-71396000	Enhancers	Fetal Kidney	kidney
49	chr1:71395800-71396200	Enhancers	Primary T cells from cord blood	blood
50	chr1:71396000-71399000	Weak transcription	Fetal Kidney	kidney

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