Variant report

Variant	nsv541561
Chromosome Location	chr12:85985510-86175711
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	chr12:86036581-86037005	HepG2	liver:	n/a	n/a
2	ATF1	chr12:86104663-86104781	K562	blood:	n/a	n/a
3	BACH1	chr12:86121439-86121442	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr12:86169235-86169489	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr12:86159050-86159743	A549	lung:	n/a	chr12:86159156-86159165
6	BRCA1	chr12:86159061-86159912	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr12:86019903-86020631	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr12:86020121-86020665	HCT-116	colon:	n/a	n/a
9	CEBPB	chr12:86036612-86036933	H1-hESC	embryonic stem cell:	n/a	chr12:86036746-86036757
10	CEBPB	chr12:86020105-86020665	HCT-116	colon:	n/a	chr12:86020651-86020662
11	CEBPB	chr12:86021300-86021775	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:86002098-86002319	A549	lung:	n/a	n/a
13	CEBPB	chr12:86068530-86068730	A549	lung:	n/a	chr12:86068595-86068606
14	CEBPB	chr12:86159102-86159751	A549	lung:	n/a	chr12:86159393-86159404
15	CEBPB	chr12:86068448-86068731	HepG2	liver:	n/a	chr12:86068595-86068606
16	CEBPB	chr12:86068475-86068698	IMR90	lung:	n/a	chr12:86068595-86068606
17	CEBPB	chr12:86159411-86159416	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:86036542-86036989	Hela-S3	cervix:	n/a	chr12:86036746-86036757
19	CEBPB	chr12:86129056-86129148	HepG2	liver:	n/a	chr12:86129111-86129122
20	CEBPB	chr12:86105778-86106085	IMR90	lung:	n/a	chr12:86105927-86105936 chr12:86105925-86105936
21	CEBPB	chr12:86002046-86002376	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:86152504-86152747	K562	blood:	n/a	chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152630 chr12:86152617-86152628
23	CEBPB	chr12:86036545-86036953	IMR90	lung:	n/a	chr12:86036746-86036757
24	CEBPB	chr12:86159241-86159616	A549	lung:	n/a	chr12:86159393-86159404
25	CEBPB	chr12:86028843-86029069	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:86021336-86021743	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:86052168-86052249	K562	blood:	n/a	n/a
28	CEBPB	chr12:86082730-86082930	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:86119774-86120117	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:86020158-86020619	A549	lung:	n/a	n/a
31	CEBPB	chr12:86036562-86036986	A549	lung:	n/a	chr12:86036746-86036757
32	CEBPB	chr12:86105751-86106119	HepG2	liver:	n/a	chr12:86105927-86105936 chr12:86105925-86105936
33	CEBPB	chr12:86060080-86060137	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:86036533-86037022	MCF-7	breast:	n/a	chr12:86036746-86036757
35	CEBPB	chr12:86152459-86152768	HepG2	liver:	n/a	chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152630 chr12:86152617-86152628
36	CEBPB	chr12:86152465-86152801	Hela-S3	cervix:	n/a	chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152630 chr12:86152617-86152628
37	CEBPB	chr12:86020007-86020716	HCT-116	colon:	n/a	chr12:86020651-86020662
38	CEBPB	chr12:86036618-86036904	HepG2	liver:	n/a	chr12:86036746-86036757
39	CEBPB	chr12:86036541-86036964	HepG2	liver:	n/a	chr12:86036746-86036757
40	CEBPB	chr12:86159191-86159685	A549	lung:	n/a	chr12:86159393-86159404
41	CEBPB	chr12:86020204-86020533	A549	lung:	n/a	n/a
42	CEBPB	chr12:86152448-86152785	A549	lung:	n/a	chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152630 chr12:86152617-86152628
43	CEBPB	chr12:86036462-86037083	HCT-116	colon:	n/a	chr12:86036746-86036757
44	CEBPB	chr12:86152463-86152770	IMR90	lung:	n/a	chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152619-86152628 chr12:86152617-86152630 chr12:86152619-86152628 chr12:86152619-86152630 chr12:86152617-86152628
45	CEBPB	chr12:86127348-86127548	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:86138632-86138905	K562	blood:	n/a	chr12:86138776-86138789 chr12:86138777-86138788 chr12:86138776-86138789
47	CEBPB	chr12:86158866-86159798	Hela-S3	cervix:	n/a	chr12:86159393-86159404 chr12:86159761-86159773
48	CEBPB	chr12:86019722-86020633	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:86149702-86149886	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:86138644-86138930	HepG2	liver:	n/a	chr12:86138776-86138789 chr12:86138777-86138788 chr12:86138776-86138789

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86040467-86040517	NHDF-neo	bronchial:	n/a
2	chr12:86040467-86040517	PANC-1	pancreas:	n/a
3	chr12:86040467-86040517	Jurkat	blood:	n/a
4	chr12:86040467-86040517	HepG2	liver:	n/a
5	chr12:86040467-86040517	SK-N-MC	brain:	n/a
6	chr12:86040467-86040517	PFSK-1	brain:	n/a
7	chr12:86040467-86040517	ECC-1	luminal epithelium:	n/a
8	chr12:86040467-86040517	NT2-D1	testis:	n/a
9	chr12:86040467-86040517	HEEpiC	esophagus:	n/a
10	chr12:86040467-86040517	Hepatocyte	liver:	n/a
11	chr12:86040467-86040517	HIPEpiC	eye:	n/a
12	chr12:86040467-86040517	AoSMC	blood vessel:	n/a
13	chr12:86040467-86040517	GM12878	blood:	n/a
14	chr12:86040467-86040517	AG09309	skin:	n/a
15	chr12:86040467-86040517	A549	lung:	n/a
16	chr12:86040467-86040517	HNPCEpiC	eye:	n/a
17	chr12:86040467-86040517	AG04450	lung:	fetal
18	chr12:86040467-86040517	GM12892	blood:	n/a
19	chr12:86040467-86040517	AG09319	gingival:	n/a
20	chr12:86040467-86040517	BJ	skin:	n/a
21	chr12:86040467-86040517	T-47D	breast:	n/a
22	chr12:86040467-86040517	ProgFib	skin:	n/a
23	chr12:86040467-86040517	Hela-S3	cervix:	n/a
24	chr12:86040467-86040517	K562	blood:	n/a
25	chr12:86040467-86040517	NB4	blood:	n/a
26	chr12:86040467-86040517	HAEpiC	amniotic membrane:	n/a
27	chr12:86040467-86040517	SKMC	muscle:	n/a
28	chr12:86040467-86040517	HL-60	blood:	n/a
29	chr12:86040467-86040517	Caco-2	colon:	n/a
30	chr12:86040467-86040517	NHBE	bronchial:	n/a
31	chr12:86040467-86040517	MCF-7	breast:	n/a
32	chr12:86040467-86040517	U87	brain:	n/a
33	chr12:86040467-86040517	HRPEpiC	eye:	n/a
34	chr12:86040467-86040517	SK-N-SH	brain:	n/a
35	chr12:86040467-86040517	IMR90	lung:	fetal
36	chr12:86040467-86040517	HRCEpiC	kidney:	n/a
37	chr12:86040467-86040517	BE2_C	brain:	n/a
38	chr12:86040467-86040517	HCM	heart:	n/a
39	chr12:86040467-86040517	HEK293	kidney:	embryo
40	chr12:86040467-86040517	MCF10A-Er-Src	breast:	n/a
41	chr12:86040467-86040517	HCPEpiC	choroid plexus:	n/a
42	chr12:86040467-86040517	HCF	heart:	n/a
43	chr12:86040467-86040517	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:86040467-86040517	LNCaP	prostate:	n/a
45	chr12:86040467-86040517	NH-A	brain:	n/a
46	chr12:86040467-86040517	HRE	kidney:	n/a
47	chr12:86040467-86040517	SAEC	small airway:	n/a
48	chr12:86040467-86040517	H1-hESC	embryonic stem cell:	embryo
49	chr12:86040467-86040517	ovcar-3	ovarian:	n/a
50	chr12:86040467-86040517	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:86039752..86042569-chr12:86049192..86051489,2	MCF-7	breast:
2	chr12:86166852..86169171-chr12:86172826..86175025,3	K562	blood:
3	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
4	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
5	chr12:86166924..86169171-chr12:86172853..86175025,2	K562	blood:
6	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
7	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
8	chr12:86036224..86038282-chr12:86040678..86042966,2	MCF-7	breast:
9	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
10	chr12:86166924..86169171-chr12:86172853..86175025,2	K562	blood:
11	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
12	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
13	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
14	chr12:86166852..86169171-chr12:86172826..86175025,3	K562	blood:
15	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASSF9-1	chr12:86175670-86176222	NONHSAT029756
2	lnc-ALX1-2	chr12:85988245-85988373	NONHSAT029750

Variant related genes	Relation type
ENSG00000263449	TF binding region
ENSG00000263449	CpG island
ENSG00000263449	chromatin interactions

Extended variants
information (count: 4611 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4611 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532380832	chr12:85985517-85985518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191757799	chr12:85985633-85985634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2199518	chr12:85985649-85985650	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs538564795	chr12:85985664-85985665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183062147	chr12:85985694-85985695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186982796	chr12:85985698-85985699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189912011	chr12:85985726-85985727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151112907	chr12:85985738-85985739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540243178	chr12:85985773-85985774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2199517	chr12:85985777-85985778	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs558898129	chr12:85985799-85985800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577163864	chr12:85985809-85985810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532689850	chr12:85985816-85985817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115636083	chr12:85985912-85985913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558853341	chr12:85985952-85985953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10863006	chr12:85985957-85985958	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs182593929	chr12:85985999-85986000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141388416	chr12:85986040-85986041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145272160	chr12:85986083-85986084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187733070	chr12:85986084-85986085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543570847	chr12:85986156-85986157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369497853	chr12:85986166-85986167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12307103	chr12:85986245-85986246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10746347	chr12:85986248-85986249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs11831266	chr12:85986268-85986269	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs137858994	chr12:85986272-85986273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142469332	chr12:85986326-85986327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555049823	chr12:85986351-85986352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370143832	chr12:85986357-85986358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60202749	chr12:85986368-85986369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs530074212	chr12:85986421-85986422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548406521	chr12:85986490-85986491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117433369	chr12:85986494-85986495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537244389	chr12:85986496-85986497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552449216	chr12:85986522-85986523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570653885	chr12:85986572-85986573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534954487	chr12:85986582-85986583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370219620	chr12:85986624-85986625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553212738	chr12:85986650-85986651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2199516	chr12:85986651-85986652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs535395629	chr12:85986684-85986685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2199515	chr12:85986695-85986696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192448404	chr12:85986743-85986744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199816056	chr12:85986787-85986788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139113411	chr12:85986788-85986789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199824645	chr12:85986789-85986790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200651216	chr12:85986790-85986791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34933683	chr12:85986791-85986792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545484116	chr12:85986801-85986802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145386089	chr12:85986928-85986929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85984200-85986200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr12:85984600-85985800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:85984600-85985800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:85984800-85985600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:85984800-85985600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr12:85984800-85985600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr12:85985800-85990000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:85990000-85990200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:85994200-85994400	Enhancers	Primary hematopoietic stem cells	blood
10	chr12:85994400-85995000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr12:85994400-85995200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:85994800-85995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:85995000-85995200	Enhancers	Primary hematopoietic stem cells	blood
14	chr12:85995200-85996400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr12:85995200-85996600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:85995400-85996800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:85996400-85998600	Enhancers	Primary hematopoietic stem cells	blood
18	chr12:85996600-85998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:85996800-85998400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:85998200-85999000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:85998200-85999000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr12:86009200-86010400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr12:86010000-86011800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:86010000-86011800	Enhancers	HepG2	liver
25	chr12:86010200-86010600	Enhancers	Fetal Brain Female	brain
26	chr12:86010400-86011600	Enhancers	Fetal Kidney	kidney
27	chr12:86010400-86011600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr12:86010800-86011800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:86011000-86011800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr12:86011200-86011400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:86011200-86011800	Enhancers	Primary hematopoietic stem cells	blood
32	chr12:86011200-86011800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr12:86011400-86012400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:86011600-86011800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr12:86011800-86014800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:86012400-86013200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:86013200-86014600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:86014600-86014800	Enhancers	NHEK	skin
39	chr12:86014600-86015200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:86014600-86015400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:86014600-86015600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:86014600-86015600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:86014800-86015200	Flanking Active TSS	NHEK	skin
44	chr12:86014800-86015400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:86014800-86015600	Enhancers	HMEC	breast
46	chr12:86015200-86015600	Enhancers	NHEK	skin
47	chr12:86015200-86020400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:86015400-86017000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:86015400-86017200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:86015600-86019600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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