Variant report

Variant	nsv899031
Chromosome Location	chr12:40520684-40580440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 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	chr12:40546628-40546911	K562	blood:	n/a	n/a
2	ATF2	chr12:40530977-40531485	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40562517-40563164	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40562547-40563179	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40561772-40562281	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40561760-40562320	GM12878	blood:	n/a	n/a
7	BATF	chr12:40561850-40562111	GM12878	blood:	n/a	chr12:40562020-40562031
8	BATF	chr12:40562763-40563054	GM12878	blood:	n/a	n/a
9	BATF	chr12:40562718-40563113	GM12878	blood:	n/a	n/a
10	BATF	chr12:40561861-40562191	GM12878	blood:	n/a	chr12:40562020-40562031
11	BATF	chr12:40531152-40531342	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:40562639-40563067	GM12878	blood:	n/a	chr12:40562817-40562826
13	BCL11A	chr12:40561855-40562181	GM12878	blood:	n/a	chr12:40562020-40562029 chr12:40562019-40562028
14	BCL11A	chr12:40562744-40562991	GM12878	blood:	n/a	chr12:40562817-40562826
15	BCLAF1	chr12:40562599-40563097	GM12878	blood:	n/a	chr12:40562817-40562826
16	BHLHE40	chr12:40561787-40563459	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:40531157-40531393	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:40564027-40564186	A549	lung:	n/a	chr12:40564105-40564116
19	CEBPB	chr12:40543763-40544037	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:40551397-40551659	A549	lung:	n/a	chr12:40551504-40551513 chr12:40551502-40551515
21	CEBPB	chr12:40535738-40536586	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:40533238-40533525	HepG2	liver:	n/a	chr12:40533360-40533371
23	CEBPB	chr12:40543731-40544102	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:40533224-40533424	A549	lung:	n/a	chr12:40533360-40533371
25	CEBPB	chr12:40558987-40559278	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:40562546-40563162	GM12878	blood:	n/a	n/a
27	CEBPB	chr12:40565470-40565502	A549	lung:	n/a	n/a
28	CEBPB	chr12:40552448-40552556	A549	lung:	n/a	n/a
29	CEBPB	chr12:40558991-40559285	A549	lung:	n/a	n/a
30	CHD1	chr12:40552572-40552917	GM12878	blood:	n/a	n/a
31	CHD2	chr12:40562672-40563107	GM12878	blood:	n/a	n/a
32	CHD2	chr12:40570471-40570477	GM12878	blood:	n/a	n/a
33	CHD2	chr12:40549674-40549874	GM12878	blood:	n/a	n/a
34	CREB1	chr12:40531137-40531390	GM12878	blood:	n/a	n/a
35	CREB1	chr12:40562700-40563169	GM12878	blood:	n/a	n/a
36	CREB1	chr12:40561823-40562211	GM12878	blood:	n/a	n/a
37	CTCF	chr12:40546720-40546870	HCM	heart:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
38	CTCF	chr12:40546583-40547061	HCT-116	colon:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
39	CTCF	chr12:40546660-40546810	GM12871	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
40	CTCF	chr12:40546700-40546850	GM12878	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
41	CTCF	chr12:40546638-40546890	MCF-7	breast:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
42	CTCF	chr12:40546680-40546830	HepG2	liver:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
43	CTCF	chr12:40547460-40547610	GM12873	blood:	n/a	n/a
44	CTCF	chr12:40546669-40546854	A549	lung:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
45	CTCF	chr12:40546680-40546830	GM12865	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
46	CTCF	chr12:40546720-40546870	AG09309	skin:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
47	CTCF	chr12:40568418-40568463	GM20000	blood:	n/a	n/a
48	CTCF	chr12:40539546-40539674	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:40557615-40557685	Lung_OC	lung:	n/a	n/a
50	CTCF	chr12:40546644-40546888	LNCaP	prostate:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40548738-40548788	AG04449	skin:	fetal
2	chr12:40548738-40548788	GM12892	blood:	n/a
3	chr12:40548738-40548788	T-47D	breast:	n/a
4	chr12:40548738-40548788	ProgFib	skin:	n/a
5	chr12:40548738-40548788	Jurkat	blood:	n/a
6	chr12:40548738-40548788	AG10803	skin:	n/a
7	chr12:40548738-40548788	GM19239	blood:	n/a
8	chr12:40548738-40548788	SAEC	small airway:	n/a
9	chr12:40548738-40548788	SK-N-MC	brain:	n/a
10	chr12:40548738-40548788	HepG2	liver:	n/a
11	chr12:40548738-40548788	PrEC	prostate:	n/a
12	chr12:40548738-40548788	HNPCEpiC	eye:	n/a
13	chr12:40548738-40548788	HIPEpiC	eye:	n/a
14	chr12:40548738-40548788	MCF-7	breast:	n/a
15	chr12:40548738-40548788	NH-A	brain:	n/a
16	chr12:40548738-40548788	Hela-S3	cervix:	n/a
17	chr12:40548738-40548788	SKMC	muscle:	n/a
18	chr12:40548738-40548788	CMK	blood:	n/a
19	chr12:40548738-40548788	HRCEpiC	kidney:	n/a
20	chr12:40548738-40548788	BE2_C	brain:	n/a
21	chr12:40548738-40548788	K562	blood:	n/a
22	chr12:40548738-40548788	NHBE	bronchial:	n/a
23	chr12:40548738-40548788	HUVEC	blood vessel:	n/a
24	chr12:40548738-40548788	GM12891	blood:	n/a
25	chr12:40548738-40548788	AoSMC	blood vessel:	n/a
26	chr12:40548738-40548788	AG09319	gingival:	n/a
27	chr12:40548738-40548788	AG04450	lung:	fetal
28	chr12:40548738-40548788	ovcar-3	ovarian:	n/a
29	chr12:40548738-40548788	NHDF-neo	bronchial:	n/a
30	chr12:40548738-40548788	SK-N-SH	brain:	n/a
31	chr12:40548738-40548788	U87	brain:	n/a
32	chr12:40548738-40548788	A549	lung:	n/a
33	chr12:40548738-40548788	HMEC	breast:	n/a
34	chr12:40548738-40548788	PFSK-1	brain:	n/a
35	chr12:40548738-40548788	ECC-1	luminal epithelium:	n/a
36	chr12:40548738-40548788	HAEpiC	amniotic membrane:	n/a
37	chr12:40548738-40548788	HL-60	blood:	n/a
38	chr12:40548738-40548788	RPTEC	kidney:	n/a
39	chr12:40548738-40548788	HEK293	kidney:	embryo
40	chr12:40548738-40548788	HCT-116	colon:	n/a
41	chr12:40548738-40548788	AG09309	skin:	n/a
42	chr12:40548738-40548788	Hepatocyte	liver:	n/a
43	chr12:40548738-40548788	HCF	heart:	n/a
44	chr12:40548738-40548788	GM06990	blood:	n/a
45	chr12:40548738-40548788	NB4	blood:	n/a
46	chr12:40548738-40548788	GM12878	blood:	n/a
47	chr12:40548738-40548788	MCF10A-Er-Src	breast:	n/a
48	chr12:40548738-40548788	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:40548738-40548788	Caco-2	colon:	n/a
50	chr12:40548738-40548788	PANC-1	pancreas:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169315069..169315689-chr12:40537506..40538182,2	MCF-7	breast:
2	chr12:40536767..40538493-chr12:40545018..40546756,2	K562	blood:
3	chr12:40536767..40538493-chr12:40545018..40546756,2	K562	blood:
4	12:40543943-40545640..12:40703633-40711447	GM12878	blood:
5	chr12:40546299..40547451-chr12:40706483..40707430,5	MCF-7	breast:
6	12:40551632-40552246..12:40691796-40694737	GM12878	blood:
7	chr12:40526853..40529105-chr12:40530805..40532717,2	MCF-7	breast:
8	chr12:40546236..40547437-chr12:40706403..40707441,12	MCF-7	breast:
9	chr12:40158520..40159448-chr12:40546284..40547792,5	MCF-7	breast:
10	chr12:40520984..40522789-chr12:40525869..40527665,2	K562	blood:
11	12:40570708-40576790..12:40691796-40694737	K562	blood:
12	chr12:40520984..40522789-chr12:40525869..40527665,2	K562	blood:
13	12:40570708-40576790..12:40703633-40711447	K562	blood:
14	chr10:125795379..125796137-chr12:40561478..40561982,2	MCF-7	breast:
15	12:40560427-40561510..12:40703633-40711447	GM12878	blood:
16	chr12:40543659..40545848-chr12:40705219..40707677,2	MCF-7	breast:
17	chr12:40526853..40529105-chr12:40530805..40532717,2	MCF-7	breast:
18	12:40545640-40549031..12:40691796-40694737	GM12878	blood:
19	12:40545640-40549031..12:40703633-40711447	GM12878	blood:
20	12:40517820-40521124..12:40703633-40711447	GM12878	blood:
21	12:40551632-40552246..12:40703633-40711447	GM12878	blood:
22	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
23	12:40525880-40532672..12:40703633-40711447	GM12878	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRK2-1	chr12:40549559-40550164	NONHSAT027720
2	lnc-LRRK2-1	chr12:40560053-40560152	NONHSAT027720
3	lnc-SLC2A13-1	chr12:40534728-40536678	ENSG00000260943.1
4	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
5	lnc-LRRK2-1	chr12:40561049-40561678	NONHSAT027720
6	lnc-SLC2A13-1	chr12:40537621-40538106	XLOC_010052
7	lnc-LRRK2-1	chr12:40561050-40561414	XLOC_009712
8	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
9	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
10	lnc-LRRK2-1	chr12:40561050-40561509	XLOC_009712
11	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
12	lnc-SLC2A13-1	chr12:40537983-40538106	XLOC_010052
13	lnc-SLC2A13-1	chr12:40534259-40536436	XLOC_010052
14	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
15	lnc-SLC2A13-2	chr12:40579811-40579985	XLOC_010053
16	lnc-LRRK2-1	chr12:40560054-40560152	XLOC_009712
17	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
18	lnc-LRRK2-1	chr12:40550041-40550145	XLOC_009712

No data

Variant related genes	Relation type
ENSG00000260943	TF binding region
ENSG00000223914	TF binding region
ENSG00000260943	CpG island
ENSG00000223914	CpG island
ENSG00000188906	chromatin interactions
BRMS1L	miRNA target sites
BRSK1	miRNA target sites
SDCBP	miRNA target sites
BRWD1	miRNA target sites
NR3C1	miRNA target sites

Extended variants
information (count: 2113 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7135678	chr12:40520684-40520685	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114708190	chr12:40520751-40520752	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575036295	chr12:40520755-40520756	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560824542	chr12:40520814-40520815	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141364528	chr12:40520923-40520924	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552711841	chr12:40520933-40520934	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536764506	chr12:40520935-40520936	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570964260	chr12:40520955-40520956	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538687702	chr12:40520974-40520975	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550689497	chr12:40521004-40521005	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192502910	chr12:40521016-40521017	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536238274	chr12:40521071-40521072	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs17489807	chr12:40521107-40521108	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573063058	chr12:40521136-40521137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533861404	chr12:40521160-40521161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550505524	chr12:40521369-40521370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542299229	chr12:40521385-40521386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185738930	chr12:40521394-40521395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562635679	chr12:40521433-40521434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35748904	chr12:40521438-40521439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552125116	chr12:40521461-40521462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574629611	chr12:40521464-40521465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570491463	chr12:40521484-40521485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146882700	chr12:40521491-40521492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4533099	chr12:40521493-40521494	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs527943425	chr12:40521534-40521535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17489820	chr12:40521543-40521544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552596707	chr12:40521550-40521551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11564137	chr12:40521587-40521588	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11564159	chr12:40521599-40521600	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575083112	chr12:40521603-40521604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550432043	chr12:40521626-40521627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149283864	chr12:40521649-40521650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79597087	chr12:40521651-40521652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28365183	chr12:40521653-40521654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28365184	chr12:40521654-40521655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201847900	chr12:40521655-40521656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs397790878	chr12:40521656-40521657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142256060	chr12:40521697-40521698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568950989	chr12:40521699-40521700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140755571	chr12:40521767-40521768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17442630	chr12:40521779-40521780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs61933163	chr12:40521822-40521823	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566355871	chr12:40521840-40521841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150087903	chr12:40521873-40521874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77099904	chr12:40521874-40521875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11175260	chr12:40521896-40521897	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs533870645	chr12:40521948-40521949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537637695	chr12:40521989-40521990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1482285	chr12:40522002-40522003	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:58)

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
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40520400-40522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:40521200-40521600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr12:40526800-40527200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr12:40526800-40527400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr12:40530600-40531400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:40530600-40531400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:40530600-40531600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:40530600-40531600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr12:40530800-40531200	Enhancers	Primary B cells from peripheral blood	blood
10	chr12:40530800-40531400	Enhancers	GM12878-XiMat	blood
11	chr12:40530800-40532000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:40531000-40531400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr12:40531000-40531400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:40531000-40531400	Enhancers	HUVEC	blood vessel
15	chr12:40531000-40531600	Enhancers	Primary B cells from cord blood	blood
16	chr12:40531200-40531600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr12:40531200-40531800	Enhancers	NHDF-Ad	bronchial
18	chr12:40531200-40532000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr12:40531200-40532400	Enhancers	HMEC	breast
20	chr12:40531400-40532600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:40531400-40532600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:40531400-40532600	Enhancers	NHEK	skin
23	chr12:40531600-40532800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:40531800-40532800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:40532400-40535600	Weak transcription	HMEC	breast
26	chr12:40532600-40535600	Weak transcription	NHEK	skin
27	chr12:40532600-40535800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:40532800-40535800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:40532800-40543800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:40533200-40533400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:40535000-40537200	Enhancers	Hela-S3	cervix
32	chr12:40535600-40536600	Enhancers	HMEC	breast
33	chr12:40535600-40536600	Enhancers	NHEK	skin
34	chr12:40535800-40536400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:40535800-40536400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:40536000-40536600	Enhancers	Placenta Amnion	Placenta Amnion
37	chr12:40540800-40541400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr12:40541000-40541800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr12:40541200-40541400	Enhancers	Aorta	Aorta
40	chr12:40541400-40546600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr12:40541800-40546600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr12:40543400-40544000	Enhancers	Adipose Nuclei	Adipose
43	chr12:40543400-40544200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:40543600-40543800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr12:40543600-40544000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:40543600-40544000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:40543600-40544000	Enhancers	Hela-S3	cervix
48	chr12:40543800-40544200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:40543800-40544200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:40543800-40544200	Enhancers	A549	lung

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