Variant report

Variant	nsv832394
Chromosome Location	chr12:45077573-45269305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:45168720-45168920	HepG2	liver:	n/a	n/a
2	ATF2	chr12:45241593-45242066	GM12878	blood:	n/a	n/a
3	BACH1	chr12:45090366-45090654	H1-hESC	embryonic stem cell:	n/a	chr12:45090508-45090522 chr12:45090490-45090504
4	BATF	chr12:45241699-45242077	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:45241674-45242071	GM12878	blood:	n/a	chr12:45241852-45241861
6	BCL3	chr12:45241703-45242043	GM12878	blood:	n/a	chr12:45241852-45241861
7	BCLAF1	chr12:45241611-45242049	GM12878	blood:	n/a	chr12:45241852-45241861
8	BHLHE40	chr12:45241695-45242020	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:45176474-45176563	GM12878	blood:	n/a	n/a
10	CBX3	chr12:45122313-45122708	HCT-116	colon:	n/a	n/a
11	CEBPB	chr12:45239858-45240058	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:45143931-45144612	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr12:45240725-45240999	HepG2	liver:	n/a	chr12:45240858-45240869
14	CEBPB	chr12:45268777-45269097	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:45172723-45172853	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:45198924-45199039	HepG2	liver:	n/a	chr12:45198982-45198993
17	CEBPB	chr12:45124793-45124930	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:45120031-45120257	A549	lung:	n/a	n/a
19	CHD1	chr12:45268922-45269885	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:45241714-45242188	GM12878	blood:	n/a	n/a
21	CHD2	chr12:45242662-45242701	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr12:45168700-45168850	GM12869	blood:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
23	CTCF	chr12:45267759-45268011	Medullo	brain:	n/a	n/a
24	CTCF	chr12:45159760-45159910	GM12873	blood:	n/a	n/a
25	CTCF	chr12:45205949-45206140	HepG2	liver:	n/a	n/a
26	CTCF	chr12:45205960-45206110	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr12:45205960-45206110	GM12866	blood:	n/a	n/a
28	CTCF	chr12:45168680-45168830	AoAF	blood vessel:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
29	CTCF	chr12:45205944-45206082	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:45159580-45159730	HepG2	liver:	n/a	n/a
31	CTCF	chr12:45267780-45267930	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:45168720-45168870	HCPEpiC	choroid plexus:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
33	CTCF	chr12:45205920-45206070	GM12869	blood:	n/a	n/a
34	CTCF	chr12:45168660-45168810	HCPEpiC	choroid plexus:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
35	CTCF	chr12:45168700-45168850	GM12873	blood:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
36	CTCF	chr12:45168661-45168913	GM10266	blood:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
37	CTCF	chr12:45159700-45159850	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr12:45267800-45267950	HAc	cerebellar:	n/a	n/a
39	CTCF	chr12:45168658-45168902	LNCaP	prostate:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
40	CTCF	chr12:45168569-45169030	A549	lung:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
41	CTCF	chr12:45168720-45168870	AG04449	skin:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
42	CTCF	chr12:45159697-45159873	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:45168561-45169008	MCF-7	breast:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
44	CTCF	chr12:45267800-45267950	HMF	breast:	n/a	n/a
45	CTCF	chr12:45267808-45267909	Lung_OC	lung:	n/a	n/a
46	CTCF	chr12:45168417-45168540	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr12:45205940-45206090	GM12864	blood:	n/a	n/a
48	CTCF	chr12:45159770-45159794	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:45168700-45168850	GM12878	blood:	n/a	chr12:45168783-45168804 chr12:45168784-45168797 chr12:45168782-45168798 chr12:45168781-45168799 chr12:45168784-45168797
50	CTCF	chr12:45205935-45205968	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:45165084-45165134	LNCaP	prostate:	n/a
2	chr12:45157448-45157498	HIPEpiC	eye:	n/a
3	chr12:45269045-45269095	Caco-2	colon:	n/a
4	chr12:45268999-45269049	MCF-7	breast:	n/a
5	chr12:45266836-45266886	AG10803	skin:	n/a
6	chr12:45269045-45269095	HNPCEpiC	eye:	n/a
7	chr12:45182192-45182242	HRCEpiC	kidney:	n/a
8	chr12:45088477-45088527	HNPCEpiC	eye:	n/a
9	chr12:45088477-45088527	HCM	heart:	n/a
10	chr12:45165084-45165134	Jurkat	blood:	n/a
11	chr12:45268999-45269049	Caco-2	colon:	n/a
12	chr12:45266836-45266886	SKMC	muscle:	n/a
13	chr12:45269045-45269095	PrEC	prostate:	n/a
14	chr12:45165084-45165134	SKMC	muscle:	n/a
15	chr12:45268613-45268663	SK-N-SH	brain:	n/a
16	chr12:45269045-45269095	U87	brain:	n/a
17	chr12:45088477-45088527	AG04450	lung:	fetal
18	chr12:45165084-45165134	CMK	blood:	n/a
19	chr12:45182192-45182242	AG09319	gingival:	n/a
20	chr12:45266836-45266886	MCF-7	breast:	n/a
21	chr12:45088477-45088527	MCF10A-Er-Src	breast:	n/a
22	chr12:45088477-45088527	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:45268999-45269049	GM06990	blood:	n/a
24	chr12:45157448-45157498	HepG2	liver:	n/a
25	chr12:45165084-45165134	HEEpiC	esophagus:	n/a
26	chr12:45165084-45165134	HCT-116	colon:	n/a
27	chr12:45182192-45182242	HCT-116	colon:	n/a
28	chr12:45266836-45266886	HRCEpiC	kidney:	n/a
29	chr12:45088477-45088527	PrEC	prostate:	n/a
30	chr12:45268999-45269049	A549	lung:	n/a
31	chr12:45266836-45266886	AoSMC	blood vessel:	n/a
32	chr12:45268999-45269049	ProgFib	skin:	n/a
33	chr12:45268999-45269049	HMEC	breast:	n/a
34	chr12:45165084-45165134	NT2-D1	testis:	n/a
35	chr12:45088477-45088527	SK-N-SH	brain:	n/a
36	chr12:45268999-45269049	GM12891	blood:	n/a
37	chr12:45157448-45157498	NT2-D1	testis:	n/a
38	chr12:45182192-45182242	MCF10A-Er-Src	breast:	n/a
39	chr12:45268613-45268663	HIPEpiC	eye:	n/a
40	chr12:45269045-45269095	HEEpiC	esophagus:	n/a
41	chr12:45088477-45088527	Jurkat	blood:	n/a
42	chr12:45157448-45157498	PFSK-1	brain:	n/a
43	chr12:45268613-45268663	K562	blood:	n/a
44	chr12:45269045-45269095	HEK293	kidney:	embryo
45	chr12:45165084-45165134	BE2_C	brain:	n/a
46	chr12:45266836-45266886	HIPEpiC	eye:	n/a
47	chr12:45182192-45182242	NT2-D1	testis:	n/a
48	chr12:45269045-45269095	A549	lung:	n/a
49	chr12:45182192-45182242	HMEC	breast:	n/a
50	chr12:45266836-45266886	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:45228113..45230766-chr12:45231414..45233959,2	K562	blood:
2	chr12:45168304..45169119-chr12:45267170..45268311,3	MCF-7	breast:
3	chr12:45228200..45231167-chr12:45235682..45238420,2	K562	blood:
4	chr12:45228200..45231167-chr12:45235682..45238420,2	K562	blood:
5	chr12:45168329..45169564-chr12:45323968..45325348,4	K562	blood:
6	chr12:45228113..45230766-chr12:45231414..45233959,2	K562	blood:
7	chr12:44859082..44859755-chr12:45083143..45083670,2	MCF-7	breast:
8	chr12:45168298..45169262-chr12:45324213..45325460,5	MCF-7	breast:
9	chr12:45206023..45206756-chr12:45324521..45325295,2	MCF-7	breast:
10	chr12:45229297..45232222-chr12:45268941..45271789,2	K562	blood:
11	chr12:45168304..45169119-chr12:45267170..45268311,3	MCF-7	breast:
12	chr12:45245058..45246783-chr12:45249459..45251550,2	MCF-7	breast:
13	chr12:44408858..44409800-chr12:45267480..45268238,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM117-4	chr12:45150203-45150316	l_632_chr12:45063675-45150311_ovary
2	lnc-TMEM117-4	chr12:45251306-45251369	l_632_chr12:45063675-45150311_ovary
3	lnc-TMEM117-4	chr12:45135059-45135191	l_632_chr12:45063675-45150311_ovary
4	lnc-TMEM117-4	chr12:45217552-45217585	l_632_chr12:45063675-45150311_ovary
5	lnc-TMEM117-4	chr12:45164508-45165212	l_632_chr12:45063675-45150311_ovary

Variant related genes	Relation type
NELL2	TF binding region
NELL2	CpG island
ENSG00000184613	chromatin interactions

Extended variants
information (count: 7516 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:7516 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1097976	chr12:45077613-45077614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186881204	chr12:45077621-45077622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561200447	chr12:45077660-45077661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191418531	chr12:45077671-45077672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146595364	chr12:45077684-45077685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565277419	chr12:45077786-45077787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532525060	chr12:45077791-45077792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182475899	chr12:45077878-45077879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189242352	chr12:45077879-45077880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193079071	chr12:45077925-45077926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530454324	chr12:45077928-45077929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548504186	chr12:45077930-45077931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139372189	chr12:45077993-45077994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185519282	chr12:45078014-45078015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558298227	chr12:45078015-45078016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570413695	chr12:45078021-45078022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537565051	chr12:45078036-45078037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189073762	chr12:45078070-45078071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575437058	chr12:45078071-45078072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192028397	chr12:45078105-45078106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555135829	chr12:45078163-45078164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573503918	chr12:45078166-45078167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201080777	chr12:45078178-45078179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540898566	chr12:45078202-45078203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565167589	chr12:45078204-45078205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557602568	chr12:45078205-45078206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532502098	chr12:45078254-45078255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372768440	chr12:45078266-45078267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558228407	chr12:45078335-45078336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562920801	chr12:45078416-45078417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530212284	chr12:45078450-45078451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374992076	chr12:45078451-45078452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548454746	chr12:45078455-45078456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560275456	chr12:45078473-45078474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527625954	chr12:45078488-45078489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9739530	chr12:45078496-45078497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570376135	chr12:45078529-45078530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537401890	chr12:45078577-45078578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11531203	chr12:45078599-45078600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561355670	chr12:45078659-45078660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7303685	chr12:45078798-45078799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567854466	chr12:45078873-45078874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535174091	chr12:45078899-45078900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570547829	chr12:45078922-45078923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372811756	chr12:45078961-45078962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188597094	chr12:45078971-45078972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554890497	chr12:45078975-45078976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573368979	chr12:45078979-45078980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144909976	chr12:45078986-45078987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562793611	chr12:45078994-45078995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45051800-45081200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr12:45056600-45083800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr12:45062400-45081200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr12:45065000-45116000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:45066800-45083000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr12:45069800-45082600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:45073400-45080800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:45073600-45080600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:45073800-45083800	Weak transcription	Fetal Brain Female	brain
10	chr12:45078800-45095600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:45080400-45081400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:45080600-45081600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:45080800-45081600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:45080800-45136000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr12:45081200-45081400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
16	chr12:45081200-45083600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr12:45081400-45088200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:45081400-45115600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr12:45081600-45084000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:45081600-45106800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:45081800-45103000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr12:45082800-45083200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:45083000-45085400	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr12:45083200-45110000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr12:45083600-45084400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr12:45083800-45085400	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr12:45083800-45085400	Strong transcription	Fetal Brain Female	brain
28	chr12:45084000-45088200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:45084400-45084800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr12:45084800-45096600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr12:45085200-45085400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:45085400-45090400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:45085400-45092000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr12:45085400-45101000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr12:45085400-45105800	Weak transcription	Fetal Brain Female	brain
36	chr12:45087600-45087800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr12:45087800-45088000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:45087800-45088000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr12:45087800-45088200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:45087800-45088200	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr12:45087800-45088600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr12:45087800-45088800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr12:45088000-45090600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr12:45088000-45110800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr12:45088200-45088400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:45088200-45088800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr12:45088200-45089600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:45088200-45089800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr12:45088400-45088800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:45088600-45090400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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