Variant report

Variant	nsv872844
Chromosome Location	chr1:194232033-194364661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:704)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:194264954-194265127	HepG2	liver:	n/a	n/a
2	ATF1	chr1:194267197-194267479	K562	blood:	n/a	n/a
3	ATF1	chr1:194343865-194344032	K562	blood:	n/a	n/a
4	ATF1	chr1:194264272-194264437	K562	blood:	n/a	n/a
5	ATF2	chr1:194258660-194259165	GM12878	blood:	n/a	n/a
6	ATF2	chr1:194258580-194259085	GM12878	blood:	n/a	n/a
7	ATF2	chr1:194249054-194249438	GM12878	blood:	n/a	n/a
8	ATF3	chr1:194312059-194312295	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:194311963-194312358	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr1:194258679-194259064	GM12878	blood:	n/a	n/a
11	BATF	chr1:194249125-194249361	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:194258667-194259124	GM12878	blood:	n/a	n/a
13	BCL3	chr1:194258709-194259079	GM12878	blood:	n/a	n/a
14	BCL3	chr1:194258639-194259038	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:194258602-194259073	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:194248979-194249416	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:194258729-194258996	GM12878	blood:	n/a	n/a
18	CEBPB	chr1:194330573-194330832	K562	blood:	n/a	chr1:194330728-194330739
19	CEBPB	chr1:194267201-194267460	A549	lung:	n/a	n/a
20	CEBPB	chr1:194267192-194267549	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:194267220-194267531	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:194267210-194267527	K562	blood:	n/a	n/a
23	CEBPB	chr1:194264750-194265141	MCF-7	breast:	n/a	n/a
24	CEBPB	chr1:194309672-194309782	A549	lung:	n/a	n/a
25	CEBPB	chr1:194267201-194267495	K562	blood:	n/a	n/a
26	CEBPB	chr1:194237780-194238333	IMR90	lung:	n/a	chr1:194238139-194238150
27	CEBPB	chr1:194237793-194238365	H1-hESC	embryonic stem cell:	n/a	chr1:194238139-194238150
28	CEBPB	chr1:194334363-194334677	HepG2	liver:	n/a	chr1:194334514-194334525
29	CEBPB	chr1:194267170-194267552	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:194330550-194330806	A549	lung:	n/a	chr1:194330728-194330739
31	CEBPB	chr1:194267200-194267535	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr1:194267110-194267655	HCT-116	colon:	n/a	n/a
33	CEBPB	chr1:194267158-194267586	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr1:194330514-194330873	Hela-S3	cervix:	n/a	chr1:194330728-194330739
35	CEBPB	chr1:194312110-194312319	A549	lung:	n/a	n/a
36	CEBPB	chr1:194334390-194334657	K562	blood:	n/a	chr1:194334514-194334525
37	CEBPB	chr1:194330473-194330868	IMR90	lung:	n/a	chr1:194330728-194330739
38	CEBPB	chr1:194273767-194273838	A549	lung:	n/a	n/a
39	CEBPB	chr1:194267190-194267539	A549	lung:	n/a	n/a
40	CEBPB	chr1:194334367-194334673	IMR90	lung:	n/a	chr1:194334514-194334525
41	CEBPB	chr1:194267151-194267568	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:194267041-194267657	HCT-116	colon:	n/a	n/a
43	CEBPB	chr1:194264833-194265042	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:194237983-194238329	Hela-S3	cervix:	n/a	chr1:194238139-194238150
45	CEBPB	chr1:194355353-194355553	HepG2	liver:	n/a	chr1:194355445-194355456 chr1:194355444-194355457
46	CEBPB	chr1:194330540-194330888	HepG2	liver:	n/a	chr1:194330728-194330739
47	CEBPB	chr1:194264851-194265147	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:194258947-194259224	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:194312007-194312285	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:194264877-194265163	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194327715-194327765	HL-60	blood:	n/a
2	chr1:194327715-194327765	HRPEpiC	eye:	n/a
3	chr1:194327715-194327765	PFSK-1	brain:	n/a
4	chr1:194327715-194327765	SK-N-SH	brain:	n/a
5	chr1:194327715-194327765	BJ	skin:	n/a
6	chr1:194327715-194327765	GM06990	blood:	n/a
7	chr1:194327715-194327765	HNPCEpiC	eye:	n/a
8	chr1:194327715-194327765	HCM	heart:	n/a
9	chr1:194327715-194327765	RPTEC	kidney:	n/a
10	chr1:194327715-194327765	HRE	kidney:	n/a
11	chr1:194327715-194327765	Caco-2	colon:	n/a
12	chr1:194327715-194327765	CMK	blood:	n/a
13	chr1:194327715-194327765	NB4	blood:	n/a
14	chr1:194327715-194327765	AG04449	skin:	fetal
15	chr1:194327715-194327765	PrEC	prostate:	n/a
16	chr1:194327715-194327765	HCF	heart:	n/a
17	chr1:194327715-194327765	SK-N-MC	brain:	n/a
18	chr1:194327715-194327765	NHBE	bronchial:	n/a
19	chr1:194327715-194327765	AG10803	skin:	n/a
20	chr1:194327715-194327765	HEEpiC	esophagus:	n/a
21	chr1:194327715-194327765	AoSMC	blood vessel:	n/a
22	chr1:194327715-194327765	SK-N-SH_RA	brain:	n/a
23	chr1:194327715-194327765	HAEpiC	amniotic membrane:	n/a
24	chr1:194327715-194327765	MCF-7	breast:	n/a
25	chr1:194327715-194327765	H1-hESC	embryonic stem cell:	embryo
26	chr1:194327715-194327765	GM12891	blood:	n/a
27	chr1:194327715-194327765	SKMC	muscle:	n/a
28	chr1:194327715-194327765	ECC-1	luminal epithelium:	n/a
29	chr1:194327715-194327765	ovcar-3	ovarian:	n/a
30	chr1:194327715-194327765	HRCEpiC	kidney:	n/a
31	chr1:194327715-194327765	LNCaP	prostate:	n/a
32	chr1:194327715-194327765	GM12878	blood:	n/a
33	chr1:194327715-194327765	HIPEpiC	eye:	n/a
34	chr1:194327715-194327765	IMR90	lung:	fetal
35	chr1:194327715-194327765	U87	brain:	n/a
36	chr1:194327715-194327765	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:194327715-194327765	NT2-D1	testis:	n/a
38	chr1:194327715-194327765	HUVEC	blood vessel:	n/a
39	chr1:194327715-194327765	GM12892	blood:	n/a
40	chr1:194327715-194327765	SAEC	small airway:	n/a
41	chr1:194327715-194327765	T-47D	breast:	n/a
42	chr1:194327715-194327765	BE2_C	brain:	n/a
43	chr1:194327715-194327765	MCF10A-Er-Src	breast:	n/a
44	chr1:194327715-194327765	HMEC	breast:	n/a
45	chr1:194327715-194327765	K562	blood:	n/a
46	chr1:194327715-194327765	AG04450	lung:	fetal
47	chr1:194327715-194327765	GM19239	blood:	n/a
48	chr1:194327715-194327765	AG09309	skin:	n/a
49	chr1:194327715-194327765	PANC-1	pancreas:	n/a
50	chr1:194327715-194327765	NHDF-neo	bronchial:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:193151512..193152776-chr1:194264703..194265563,3	MCF-7	breast:
2	chr1:194259902..194262813-chr1:194263543..194265808,3	K562	blood:
3	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
4	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
5	chr1:194259902..194262813-chr1:194263543..194265808,3	K562	blood:
6	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
7	chr1:194071422..194072384-chr1:194264231..194265518,7	MCF-7	breast:
8	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
9	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
10	chr1:194249167..194252027-chr1:194255378..194258049,2	MCF-7	breast:
11	chr1:194070430..194072677-chr1:194322592..194324190,2	K562	blood:
12	chr1:193375639..193376499-chr1:194264953..194265474,2	MCF-7	breast:
13	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
14	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
15	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:
16	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
17	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
18	chr1:194256252..194258027-chr1:194260432..194262987,2	K562	blood:
19	chr1:193587120..193589760-chr1:194326578..194328851,2	K562	blood:
20	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
21	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
22	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
23	chr1:194128824..194129656-chr1:194264555..194265184,3	MCF-7	breast:
24	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
25	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:
26	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
27	chr1:194237234..194239650-chr1:194241367..194244055,3	K562	blood:
28	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
29	chr1:194237234..194239650-chr1:194241367..194244055,3	K562	blood:
30	chr1:194256252..194258027-chr1:194260432..194262987,2	K562	blood:
31	chr1:194128967..194129865-chr1:194264643..194265551,3	MCF-7	breast:
32	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
33	chr1:194266672..194269041-chr1:194271611..194273227,2	K562	blood:
34	chr1:193576702..193577442-chr1:194264619..194265502,2	MCF-7	breast:
35	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
36	chr1:194072910..194073570-chr1:194264512..194265049,2	MCF-7	breast:
37	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:
38	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
39	chr1:194266672..194269041-chr1:194271611..194273227,2	K562	blood:
40	chr1:194315164..194317998-chr1:194319254..194321893,3	K562	blood:
41	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
42	chr1:194308962..194311330-chr4:127715408..127718280,2	MCF-7	breast:
43	chr1:194249167..194252027-chr1:194255378..194258049,2	MCF-7	breast:
44	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
45	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GALT2-5	chr1:194296750-194296826	NONHSAT008580
2	lnc-B3GALT2-5	chr1:194280749-194281292	NONHSAT008580
3	lnc-CDC73-4	chr1:194320009-194320481	NONHSAT008581
4	lnc-CDC73-4	chr1:194320593-194321556	NONHSAT008581
5	lnc-CDC73-4	chr1:194320073-194320368	XLOC_000510
6	lnc-CDC73-4	chr1:194321413-194321556	XLOC_000510

No data

Variant related genes	Relation type
ENSG00000231714	TF binding region
ENSG00000231714	CpG island
ENSG00000231714	chromatin interactions

Extended variants
information (count: 2322 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs626245	chr1:194232033-194232034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541073201	chr1:194232041-194232042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559410529	chr1:194232048-194232049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574869974	chr1:194232074-194232075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78163436	chr1:194232105-194232106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563696544	chr1:194232133-194232134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs589999	chr1:194232134-194232135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs79513293	chr1:194232141-194232142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12080305	chr1:194232144-194232145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536965254	chr1:194232148-194232149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532137152	chr1:194232161-194232162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192379209	chr1:194232186-194232187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565749796	chr1:194232194-194232195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535940571	chr1:194232195-194232196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567890759	chr1:194232233-194232234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548278562	chr1:194232248-194232249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs590482	chr1:194232252-194232253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs590510	chr1:194232277-194232278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377048593	chr1:194232282-194232283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183293838	chr1:194232294-194232295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570453599	chr1:194232311-194232312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534681659	chr1:194232315-194232316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552977970	chr1:194232361-194232362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149260477	chr1:194232381-194232382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541918231	chr1:194232437-194232438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201079914	chr1:194232441-194232442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202185604	chr1:194232452-194232453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4466636	chr1:194232454-194232455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557431772	chr1:194232459-194232460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145334210	chr1:194232464-194232465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370113317	chr1:194232467-194232468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546462080	chr1:194232471-194232472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs137906830	chr1:194232502-194232503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528824643	chr1:194232507-194232508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142327353	chr1:194232513-194232514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146162740	chr1:194232526-194232527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543452281	chr1:194232529-194232530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4623674	chr1:194232548-194232549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73055100	chr1:194232573-194232574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372844735	chr1:194232593-194232594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140165395	chr1:194232594-194232595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141534406	chr1:194232649-194232650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188692721	chr1:194232658-194232659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192535643	chr1:194232713-194232714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114955946	chr1:194232762-194232763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568317582	chr1:194232777-194232778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182697457	chr1:194232818-194232819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2477613	chr1:194232913-194232914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557165932	chr1:194232981-194232982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186624324	chr1:194232993-194232994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194232000-194233600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:194233000-194233200	ZNF genes & repeats	Thymus	Thymus
3	chr1:194233000-194233800	ZNF genes & repeats	Fetal Thymus	thymus
4	chr1:194233200-194234000	Strong transcription	Thymus	Thymus
5	chr1:194233600-194234600	Strong transcription	Primary T cells from cord blood	blood
6	chr1:194233800-194249600	Weak transcription	Fetal Thymus	thymus
7	chr1:194234000-194235600	Weak transcription	Thymus	Thymus
8	chr1:194234600-194250200	Weak transcription	Primary T cells from cord blood	blood
9	chr1:194237800-194238600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:194237800-194238600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:194237800-194238600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr1:194238200-194238600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:194249000-194250000	Enhancers	Primary B cells from cord blood	blood
14	chr1:194249600-194249800	Enhancers	Fetal Thymus	thymus
15	chr1:194249600-194250400	Enhancers	GM12878-XiMat	blood
16	chr1:194249800-194250200	Weak transcription	Fetal Thymus	thymus
17	chr1:194249800-194250800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:194250200-194251200	Enhancers	Primary T cells from cord blood	blood
19	chr1:194250400-194251000	Enhancers	Fetal Heart	heart
20	chr1:194250800-194251000	Enhancers	Primary B cells from cord blood	blood
21	chr1:194250800-194251800	Enhancers	Colon Smooth Muscle	Colon
22	chr1:194250800-194255000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:194251200-194256800	Weak transcription	Primary T cells from cord blood	blood
24	chr1:194255000-194255200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr1:194255000-194255400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:194255000-194255400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:194255400-194256400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr1:194255400-194258600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:194256400-194256600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr1:194256400-194257400	Enhancers	Primary T cells fromperipheralblood	blood
31	chr1:194256400-194257400	Enhancers	Fetal Thymus	thymus
32	chr1:194256600-194258600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:194256800-194257000	Enhancers	Primary T cells from cord blood	blood
34	chr1:194256800-194258600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr1:194256800-194259000	Active TSS	Thymus	Thymus
36	chr1:194257000-194257800	Weak transcription	Primary T cells from cord blood	blood
37	chr1:194257200-194258800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:194257400-194257600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:194257400-194258000	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr1:194257400-194258200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr1:194257400-194258800	Active TSS	Fetal Thymus	thymus
42	chr1:194257600-194258600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:194257800-194258000	Bivalent Enhancer	Primary B cells from cord blood	blood
44	chr1:194257800-194258000	Enhancers	Primary T cells from cord blood	blood
45	chr1:194257800-194258000	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr1:194257800-194258000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:194257800-194258200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr1:194258000-194258200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr1:194258000-194258600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:194258000-194258600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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