Variant report

Variant	nsv428591
Chromosome Location	chr12:60446360-60631044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:61)
Chromatin interactive
region (count:87)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:60535077-60535088	K562	blood:	n/a	n/a
2	ARID3A	chr12:60541815-60542438	K562	blood:	n/a	n/a
3	ARID3A	chr12:60562277-60562601	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:60516253-60516435	K562	blood:	n/a	n/a
5	ARID3A	chr12:60537430-60538660	K562	blood:	n/a	chr12:60537712-60537728
6	ATF1	chr12:60538204-60538547	K562	blood:	n/a	n/a
7	ATF1	chr12:60471816-60472199	K562	blood:	n/a	n/a
8	BACH1	chr12:60532359-60532629	K562	blood:	n/a	n/a
9	BACH1	chr12:60599273-60599980	K562	blood:	n/a	n/a
10	BACH1	chr12:60580498-60580551	K562	blood:	n/a	n/a
11	BACH1	chr12:60598979-60599692	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:60531305-60531407	K562	blood:	n/a	n/a
13	BHLHE40	chr12:60538230-60538531	K562	blood:	n/a	n/a
14	BHLHE40	chr12:60562301-60562557	K562	blood:	n/a	n/a
15	BHLHE40	chr12:60562274-60562618	HepG2	liver:	n/a	n/a
16	BHLHE40	chr12:60471887-60471910	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:60541969-60542355	K562	blood:	n/a	n/a
18	BHLHE40	chr12:60513331-60513358	K562	blood:	n/a	n/a
19	CBX3	chr12:60607700-60608071	K562	blood:	n/a	n/a
20	CBX3	chr12:60606354-60606787	K562	blood:	n/a	n/a
21	CBX3	chr12:60501770-60502080	K562	blood:	n/a	n/a
22	CBX3	chr12:60519937-60520277	K562	blood:	n/a	n/a
23	CCNT2	chr12:60538138-60538631	K562	blood:	n/a	n/a
24	CEBPB	chr12:60563683-60564061	IMR90	lung:	n/a	n/a
25	CEBPB	chr12:60487941-60488315	Hela-S3	cervix:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
26	CEBPB	chr12:60588522-60588817	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr12:60562226-60562613	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:60538132-60538442	K562	blood:	n/a	n/a
29	CEBPB	chr12:60606000-60606252	H1-hESC	embryonic stem cell:	n/a	chr12:60606132-60606143
30	CEBPB	chr12:60591343-60591731	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:60542628-60542961	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:60605954-60606305	IMR90	lung:	n/a	chr12:60606132-60606143
33	CEBPB	chr12:60593197-60593271	K562	blood:	n/a	n/a
34	CEBPB	chr12:60591424-60591770	A549	lung:	n/a	n/a
35	CEBPB	chr12:60567341-60567768	ECC-1	luminal epithelium:	n/a	chr12:60567548-60567559 chr12:60567423-60567434
36	CEBPB	chr12:60526140-60526175	K562	blood:	n/a	n/a
37	CEBPB	chr12:60567158-60567749	HepG2	liver:	n/a	chr12:60567548-60567559 chr12:60567423-60567434
38	CEBPB	chr12:60567441-60567657	HepG2	liver:	n/a	chr12:60567548-60567559
39	CEBPB	chr12:60505966-60506178	A549	lung:	n/a	n/a
40	CEBPB	chr12:60567281-60567816	K562	blood:	n/a	chr12:60567548-60567559 chr12:60567423-60567434
41	CEBPB	chr12:60605962-60606307	A549	lung:	n/a	chr12:60606132-60606143
42	CEBPB	chr12:60567228-60567819	A549	lung:	n/a	chr12:60567548-60567559 chr12:60567423-60567434
43	CEBPB	chr12:60505870-60506180	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr12:60532310-60532417	HepG2	liver:	n/a	chr12:60532347-60532358
45	CEBPB	chr12:60488079-60488301	A549	lung:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
46	CEBPB	chr12:60562273-60562632	MCF-7	breast:	n/a	n/a
47	CEBPB	chr12:60517185-60517778	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr12:60502756-60503018	K562	blood:	n/a	n/a
49	CEBPB	chr12:60563722-60563972	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:60567161-60567987	H1-hESC	embryonic stem cell:	n/a	chr12:60567548-60567559 chr12:60567423-60567434

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60567672-60567722	HAEpiC	amniotic membrane:	n/a
2	chr12:60567672-60567722	SAEC	small airway:	n/a
3	chr12:60567672-60567722	AG09309	skin:	n/a
4	chr12:60567672-60567722	AG04450	lung:	fetal
5	chr12:60567672-60567722	NH-A	brain:	n/a
6	chr12:60567672-60567722	PANC-1	pancreas:	n/a
7	chr12:60567672-60567722	MCF10A-Er-Src	breast:	n/a
8	chr12:60567672-60567722	AG04449	skin:	fetal
9	chr12:60567672-60567722	AG10803	skin:	n/a
10	chr12:60567672-60567722	AoSMC	blood vessel:	n/a
11	chr12:60567672-60567722	H1-hESC	embryonic stem cell:	embryo
12	chr12:60567672-60567722	ECC-1	luminal epithelium:	n/a
13	chr12:60567672-60567722	BE2_C	brain:	n/a
14	chr12:60567672-60567722	IMR90	lung:	fetal
15	chr12:60567672-60567722	A549	lung:	n/a
16	chr12:60567672-60567722	HRE	kidney:	n/a
17	chr12:60567672-60567722	GM12878	blood:	n/a
18	chr12:60567672-60567722	CMK	blood:	n/a
19	chr12:60567672-60567722	GM06990	blood:	n/a
20	chr12:60567672-60567722	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:60567672-60567722	HUVEC	blood vessel:	n/a
22	chr12:60567672-60567722	Caco-2	colon:	n/a
23	chr12:60567672-60567722	BJ	skin:	n/a
24	chr12:60567672-60567722	MCF-7	breast:	n/a
25	chr12:60567672-60567722	NT2-D1	testis:	n/a
26	chr12:60567672-60567722	SK-N-SH_RA	brain:	n/a
27	chr12:60567672-60567722	PrEC	prostate:	n/a
28	chr12:60567672-60567722	NB4	blood:	n/a
29	chr12:60567672-60567722	HEEpiC	esophagus:	n/a
30	chr12:60567672-60567722	SK-N-SH	brain:	n/a
31	chr12:60567672-60567722	GM12892	blood:	n/a
32	chr12:60567672-60567722	Hepatocyte	liver:	n/a
33	chr12:60567672-60567722	HCT-116	colon:	n/a
34	chr12:60567672-60567722	HL-60	blood:	n/a
35	chr12:60567672-60567722	GM19239	blood:	n/a
36	chr12:60567672-60567722	ovcar-3	ovarian:	n/a
37	chr12:60567672-60567722	ProgFib	skin:	n/a
38	chr12:60567672-60567722	HRCEpiC	kidney:	n/a
39	chr12:60567672-60567722	RPTEC	kidney:	n/a
40	chr12:60567672-60567722	Jurkat	blood:	n/a
41	chr12:60567672-60567722	SK-N-MC	brain:	n/a
42	chr12:60567672-60567722	HIPEpiC	eye:	n/a
43	chr12:60567672-60567722	SKMC	muscle:	n/a
44	chr12:60567672-60567722	PFSK-1	brain:	n/a
45	chr12:60567672-60567722	HRPEpiC	eye:	n/a
46	chr12:60567672-60567722	HNPCEpiC	eye:	n/a
47	chr12:60567672-60567722	HepG2	liver:	n/a
48	chr12:60567672-60567722	HEK293	kidney:	embryo
49	chr12:60567672-60567722	T-47D	breast:	n/a
50	chr12:60567672-60567722	HCF	heart:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:60563916..60564532-chr5:120756222..120756804,2	MCF-7	breast:
2	chr12:60540647..60543131-chr12:62652569..62655278,2	K562	blood:
3	chr12:60618343..60621126-chr12:60626105..60627669,2	K562	blood:
4	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
5	chr12:60610771..60614544-chr12:60615184..60617062,3	K562	blood:
6	chr12:60591422..60593897-chr12:60595165..60597772,2	K562	blood:
7	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
8	chr12:60545261..60548162-chr12:60566803..60568706,2	K562	blood:
9	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
10	chr12:60578463..60581304-chr12:60589839..60591581,2	MCF-7	breast:
11	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
12	chr12:60569954..60572860-chr12:60574344..60576067,2	K562	blood:
13	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
14	chr12:60567857..60570326-chr12:60575154..60577967,2	K562	blood:
15	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
16	chr12:60567260..60569470-chr12:60576239..60579233,2	MCF-7	breast:
17	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
18	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
19	chr12:60550084..60551908-chr12:60553624..60555521,2	MCF-7	breast:
20	chr12:60591422..60593897-chr12:60595165..60597772,2	K562	blood:
21	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
22	chr12:60532105..60534089-chr12:60535432..60537757,2	K562	blood:
23	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
24	chr12:60558094..60560220-chr12:60756513..60758831,2	MCF-7	breast:
25	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
26	chr12:60554713..60557488-chr12:60585301..60588073,2	MCF-7	breast:
27	chr12:60573054..60574989-chr12:60578511..60580681,2	MCF-7	breast:
28	chr12:60504072..60505898-chr12:60508585..60511528,2	K562	blood:
29	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
30	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
31	chr12:60541351..60544237-chr12:60546904..60548454,2	K562	blood:
32	chr12:60610562..60614544-chr12:60614554..60617623,4	K562	blood:
33	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
34	chr12:60539977..60540691-chr18:58172003..58172727,2	MCF-7	breast:
35	chr12:60556765..60558299-chr12:60600713..60603668,2	K562	blood:
36	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
37	chr12:60540346..60541953-chr12:60546209..60549149,2	MCF-7	breast:
38	chr12:60464696..60468583-chr12:60490353..60494821,4	MCF-7	breast:
39	chr12:60540346..60541953-chr12:60546209..60549149,2	MCF-7	breast:
40	chr12:60556765..60558299-chr12:60600713..60603668,2	K562	blood:
41	chr12:60617591..60619683-chr12:60621297..60623226,2	MCF-7	breast:
42	chr12:60583733..60585895-chr12:60586896..60588579,2	MCF-7	breast:
43	chr12:60618343..60621126-chr12:60626105..60627669,2	K562	blood:
44	chr12:60493772..60496447-chr12:60496844..60499476,2	K562	blood:
45	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
46	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
47	chr12:60554713..60557488-chr12:60585301..60588073,2	MCF-7	breast:
48	chr12:60481263..60483527-chr12:60485827..60488653,2	K562	blood:
49	chr12:60567857..60570326-chr12:60575154..60577967,2	K562	blood:
50	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A7-2	chr12:60488910-60489632	ENSG00000257294
2	lnc-SLC16A7-2	chr12:60486645-60486690	ENSG00000257294

No data

Variant related genes	Relation type
ENSG00000258184	TF binding region
ENSG00000257294	TF binding region
ENSG00000258184	CpG island
ENSG00000257294	CpG island
ENSG00000198673	chromatin interactions
ENSG00000135655	chromatin interactions
ENSG00000251822	chromatin interactions
ENSG00000257294	chromatin interactions

Extended variants
information (count: 5595 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5595 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140797440	chr12:60453830-60453831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533314467	chr12:60453831-60453832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547166482	chr12:60453881-60453882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566866616	chr12:60453898-60453899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12369823	chr12:60453909-60453910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368110174	chr12:60453913-60453914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535733391	chr12:60453918-60453919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139812040	chr12:60453959-60453960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547812562	chr12:60453982-60453983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567692833	chr12:60453986-60453987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537166582	chr12:60453994-60453995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556741075	chr12:60454026-60454027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531848325	chr12:60454052-60454053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576972895	chr12:60454062-60454063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539301892	chr12:60454095-60454096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143026553	chr12:60454145-60454146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573201804	chr12:60454149-60454150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545047184	chr12:60454157-60454158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11173308	chr12:60454177-60454178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562079248	chr12:60454190-60454191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575506558	chr12:60454218-60454219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544693159	chr12:60454234-60454235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564467984	chr12:60454236-60454237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144677002	chr12:60454240-60454241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546914603	chr12:60454243-60454244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560293605	chr12:60454275-60454276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187260333	chr12:60454281-60454282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374777769	chr12:60454286-60454287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17123263	chr12:60454295-60454296	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs148701283	chr12:60454324-60454325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530379231	chr12:60454377-60454378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111393145	chr12:60454398-60454399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530188819	chr12:60454405-60454406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570495996	chr12:60454441-60454442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539496628	chr12:60454466-60454467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553224561	chr12:60454479-60454480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573307056	chr12:60454489-60454490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566636851	chr12:60454539-60454540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74681675	chr12:60454572-60454573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375533747	chr12:60454595-60454596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555651165	chr12:60454628-60454629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369478138	chr12:60454659-60454660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374529381	chr12:60454660-60454661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544318888	chr12:60454682-60454683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558118861	chr12:60454684-60454685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11173309	chr12:60454801-60454802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs78003781	chr12:60454807-60454808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560332288	chr12:60454877-60454878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs968106	chr12:60454892-60454893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs542917447	chr12:60454907-60454908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60453800-60454600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:60454000-60454600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:60454000-60454600	Enhancers	NHEK	skin
4	chr12:60454200-60454400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:60454400-60464000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:60455600-60456000	Enhancers	Fetal Intestine Small	intestine
7	chr12:60464000-60464200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:60464000-60464200	Enhancers	HMEC	breast
9	chr12:60464000-60464600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:60464000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:60464000-60467400	Enhancers	NHEK	skin
12	chr12:60464200-60465200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:60464200-60465200	Weak transcription	HMEC	breast
14	chr12:60464200-60466800	Enhancers	HUVEC	blood vessel
15	chr12:60464400-60464600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:60464400-60464600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:60464600-60465000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:60464600-60465600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:60465000-60466200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:60465000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:60465200-60465800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr12:60465200-60467000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:60465200-60467000	Enhancers	HMEC	breast
24	chr12:60465600-60467000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:60465800-60467600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr12:60466000-60466400	Enhancers	Aorta	Aorta
27	chr12:60466000-60467400	Enhancers	NH-A	brain
28	chr12:60466200-60467400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:60466200-60467400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:60466400-60467000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:60466400-60467600	Enhancers	Fetal Heart	heart
32	chr12:60466600-60467000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr12:60466600-60467400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:60466600-60467400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr12:60466600-60468200	Enhancers	NHDF-Ad	bronchial
36	chr12:60467000-60467400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:60467000-60467400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr12:60467000-60475200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:60467400-60469000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:60467600-60471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:60467800-60468200	Enhancers	Fetal Muscle Leg	muscle
42	chr12:60469000-60469200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:60471400-60471800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:60471400-60473000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr12:60471600-60473000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:60471800-60472000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr12:60471800-60472200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:60472200-60472800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:60475000-60475400	Enhancers	HUVEC	blood vessel
50	chr12:60475000-60476400	Enhancers	NHEK	skin

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