Variant report

Variant	nsv898872
Chromosome Location	chr12:21000586-21413632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:305)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:21392742-21392928	K562	blood:	n/a	n/a
2	ATF1	chr12:21387015-21387268	K562	blood:	n/a	n/a
3	BACH1	chr12:21322799-21322999	K562	blood:	n/a	n/a
4	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:21380331-21380521	K562	blood:	n/a	n/a
6	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
7	BATF	chr12:21090344-21090547	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:21017099-21017177	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:21138511-21138625	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:21103222-21103500	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
14	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
15	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
16	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
17	CEBPB	chr12:21036323-21036549	HepG2	liver:	n/a	chr12:21036463-21036474
18	CEBPB	chr12:21409453-21409717	HepG2	liver:	n/a	chr12:21409600-21409611
19	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
20	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
21	CEBPB	chr12:21056070-21056238	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:21356519-21356864	IMR90	lung:	n/a	chr12:21356695-21356706
23	CEBPB	chr12:21193602-21193866	HepG2	liver:	n/a	chr12:21193754-21193765
24	CEBPB	chr12:21260031-21260260	IMR90	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
25	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
26	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
27	CEBPB	chr12:21410877-21411098	A549	lung:	n/a	n/a
28	CEBPB	chr12:21356602-21356832	H1-hESC	embryonic stem cell:	n/a	chr12:21356695-21356706
29	CEBPB	chr12:21243024-21243307	HepG2	liver:	n/a	chr12:21243166-21243177
30	CEBPB	chr12:21175943-21176096	H1-hESC	embryonic stem cell:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
31	CEBPB	chr12:21133477-21133530	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:21297827-21298053	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
34	CEBPB	chr12:21037942-21038507	A549	lung:	n/a	n/a
35	CEBPB	chr12:21233354-21233510	A549	lung:	n/a	n/a
36	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
37	CEBPB	chr12:21114301-21114316	A549	lung:	n/a	n/a
38	CEBPB	chr12:21358486-21358919	A549	lung:	n/a	n/a
39	CEBPB	chr12:21356579-21356809	HepG2	liver:	n/a	chr12:21356695-21356706
40	CEBPB	chr12:21394755-21395080	A549	lung:	n/a	chr12:21394924-21394935
41	CEBPB	chr12:21409557-21409626	K562	blood:	n/a	chr12:21409600-21409611
42	CEBPB	chr12:21282343-21282678	HepG2	liver:	n/a	chr12:21282598-21282609 chr12:21282528-21282539
43	CEBPB	chr12:21168771-21169100	A549	lung:	n/a	chr12:21168919-21168930
44	CEBPB	chr12:21193579-21193868	A549	lung:	n/a	chr12:21193754-21193765
45	CEBPB	chr12:21409481-21409705	A549	lung:	n/a	chr12:21409600-21409611
46	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
47	CEBPB	chr12:21246783-21246933	HepG2	liver:	n/a	chr12:21246828-21246839
48	CEBPB	chr12:21193722-21193901	H1-hESC	embryonic stem cell:	n/a	chr12:21193754-21193765
49	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
50	CEBPB	chr12:21234048-21234229	H1-hESC	embryonic stem cell:	n/a	chr12:21234179-21234190

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21283725-21283775	GM12892	blood:	n/a
2	chr12:21014317-21014367	MCF-7	breast:	n/a
3	chr12:21287375-21287425	ECC-1	luminal epithelium:	n/a
4	chr12:21287375-21287425	Hepatocyte	liver:	n/a
5	chr12:21287375-21287425	SKMC	muscle:	n/a
6	chr12:21287375-21287425	BE2_C	brain:	n/a
7	chr12:21283725-21283775	AG04449	skin:	fetal
8	chr12:21015340-21015390	NHBE	bronchial:	n/a
9	chr12:21014317-21014367	GM12891	blood:	n/a
10	chr12:21283725-21283775	HAEpiC	amniotic membrane:	n/a
11	chr12:21324585-21324635	HepG2	liver:	n/a
12	chr12:21283725-21283775	HMEC	breast:	n/a
13	chr12:21283725-21283775	AG09309	skin:	n/a
14	chr12:21015340-21015390	Jurkat	blood:	n/a
15	chr12:21014317-21014367	PrEC	prostate:	n/a
16	chr12:21015340-21015390	AG10803	skin:	n/a
17	chr12:21287375-21287425	AG04449	skin:	fetal
18	chr12:21014317-21014367	T-47D	breast:	n/a
19	chr12:21324585-21324635	HRCEpiC	kidney:	n/a
20	chr12:21014317-21014367	HepG2	liver:	n/a
21	chr12:21014317-21014367	HNPCEpiC	eye:	n/a
22	chr12:21015340-21015390	AG09309	skin:	n/a
23	chr12:21287375-21287425	SK-N-SH	brain:	n/a
24	chr12:21287375-21287425	HUVEC	blood vessel:	n/a
25	chr12:21015340-21015390	SKMC	muscle:	n/a
26	chr12:21324585-21324635	SK-N-MC	brain:	n/a
27	chr12:21283725-21283775	AG04450	lung:	fetal
28	chr12:21014317-21014367	NHDF-neo	bronchial:	n/a
29	chr12:21283725-21283775	NHBE	bronchial:	n/a
30	chr12:21015340-21015390	AoSMC	blood vessel:	n/a
31	chr12:21014317-21014367	AoSMC	blood vessel:	n/a
32	chr12:21287375-21287425	GM12878	blood:	n/a
33	chr12:21283725-21283775	PFSK-1	brain:	n/a
34	chr12:21324585-21324635	NH-A	brain:	n/a
35	chr12:21014317-21014367	PFSK-1	brain:	n/a
36	chr12:21324585-21324635	Hela-S3	cervix:	n/a
37	chr12:21015340-21015390	U87	brain:	n/a
38	chr12:21014317-21014367	HIPEpiC	eye:	n/a
39	chr12:21287375-21287425	A549	lung:	n/a
40	chr12:21287375-21287425	Hela-S3	cervix:	n/a
41	chr12:21324585-21324635	BJ	skin:	n/a
42	chr12:21287375-21287425	Caco-2	colon:	n/a
43	chr12:21014317-21014367	AG09309	skin:	n/a
44	chr12:21283725-21283775	HL-60	blood:	n/a
45	chr12:21287375-21287425	IMR90	lung:	fetal
46	chr12:21283725-21283775	U87	brain:	n/a
47	chr12:21015340-21015390	SK-N-SH	brain:	n/a
48	chr12:21283725-21283775	NH-A	brain:	n/a
49	chr12:21015340-21015390	ovcar-3	ovarian:	n/a
50	chr12:21015340-21015390	AG04450	lung:	fetal

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
2	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
3	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
4	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
5	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
6	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
7	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
8	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
9	chr12:21193958..21195458-chr17:59872939..59874521,2	MCF-7	breast:
10	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
11	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
12	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
13	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
14	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
15	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
16	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
17	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
18	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:
19	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:
20	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
21	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
22	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
23	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
24	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
25	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
26	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
27	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
28	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
29	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
30	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1B1-1	chr12:21220285-21220317	NONHSAT027240
2	lnc-SLCO1A2-5	chr12:21083248-21084757	NONHSAT027238
3	lnc-SLCO1B1-1	chr12:21228194-21228718	NONHSAT027240

No data

Variant related genes	Relation type
SLCO1B3	TF binding region
ENSG00000257062	TF binding region
SLCO1B1	TF binding region
SLCO1B7	TF binding region
SLCO1B3	CpG island
ENSG00000257062	CpG island
SLCO1B1	CpG island
SLCO1B7	CpG island

Extended variants
information (count: 13121 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:13121 , 50 per page) page: 1 2 3 4 5 6 7 ... 263

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1304608	chr12:21000586-21000587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149425950	chr12:21000632-21000633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35543005	chr12:21000633-21000634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183651687	chr12:21000637-21000638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150073509	chr12:21000642-21000643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs71043206	chr12:21000648-21000649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547808739	chr12:21000664-21000665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561342948	chr12:21000667-21000668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528013197	chr12:21000672-21000673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7137175	chr12:21000731-21000732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs570960027	chr12:21000806-21000807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6487155	chr12:21000893-21000894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556053437	chr12:21000901-21000902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550311840	chr12:21000938-21000939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570196780	chr12:21000961-21000962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6487156	chr12:21000974-21000975	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555846693	chr12:21000985-21000986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190716531	chr12:21001049-21001050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373099400	chr12:21001064-21001065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397693709	chr12:21001065-21001066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201202654	chr12:21001066-21001067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533854576	chr12:21001131-21001132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553990230	chr12:21001132-21001133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576987876	chr12:21001181-21001182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368598760	chr12:21001184-21001185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372898078	chr12:21001198-21001199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545949223	chr12:21001209-21001210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75702242	chr12:21001223-21001224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555915881	chr12:21001226-21001227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575778189	chr12:21001234-21001235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577023737	chr12:21001239-21001240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140652639	chr12:21001308-21001309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561353588	chr12:21001353-21001354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76658007	chr12:21001397-21001398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541381060	chr12:21001476-21001477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564767360	chr12:21001491-21001492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142794821	chr12:21001519-21001520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77623573	chr12:21001529-21001530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10770751	chr12:21001546-21001547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs10770752	chr12:21001563-21001564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs10841671	chr12:21001568-21001569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565946093	chr12:21001577-21001578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534990875	chr12:21001603-21001604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151044164	chr12:21001606-21001607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570760090	chr12:21001663-21001664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539342206	chr12:21001698-21001699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536395365	chr12:21001782-21001783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555977383	chr12:21001787-21001788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139761047	chr12:21001802-21001803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556587487	chr12:21001811-21001812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20996000-21004800	Weak transcription	Liver	Liver
2	chr12:21004800-21005000	ZNF genes & repeats	Liver	Liver
3	chr12:21006200-21011000	Weak transcription	Liver	Liver
4	chr12:21006600-21018000	Weak transcription	A549	lung
5	chr12:21007200-21007800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:21007400-21007800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr12:21007400-21007800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr12:21007400-21008200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr12:21007600-21008000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr12:21011000-21014600	Strong transcription	Liver	Liver
11	chr12:21014600-21015400	Weak transcription	Liver	Liver
12	chr12:21015400-21018400	Strong transcription	Liver	Liver
13	chr12:21017800-21019200	Enhancers	HUVEC	blood vessel
14	chr12:21018000-21018200	Strong transcription	A549	lung
15	chr12:21018200-21018800	Weak transcription	A549	lung
16	chr12:21018400-21020800	Weak transcription	Liver	Liver
17	chr12:21018800-21020600	Strong transcription	A549	lung
18	chr12:21019800-21020000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:21020000-21020400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:21020000-21020600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:21020600-21021600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:21020600-21027400	Weak transcription	A549	lung
23	chr12:21020800-21021200	Strong transcription	Liver	Liver
24	chr12:21020800-21021600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:21021200-21024600	Weak transcription	Liver	Liver
26	chr12:21021600-21022200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:21024600-21026200	Strong transcription	Liver	Liver
28	chr12:21026200-21027800	Weak transcription	Liver	Liver
29	chr12:21027400-21028400	Strong transcription	A549	lung
30	chr12:21027800-21029600	Strong transcription	Liver	Liver
31	chr12:21028400-21035800	Weak transcription	A549	lung
32	chr12:21029600-21032400	Weak transcription	Liver	Liver
33	chr12:21032400-21035400	Strong transcription	Liver	Liver
34	chr12:21034000-21034200	Enhancers	Rectal Smooth Muscle	rectum
35	chr12:21034400-21035000	Enhancers	Stomach Mucosa	stomach
36	chr12:21034400-21035600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr12:21035000-21035400	Weak transcription	Stomach Mucosa	stomach
38	chr12:21035400-21036000	Enhancers	Stomach Mucosa	stomach
39	chr12:21035400-21039000	Weak transcription	Liver	Liver
40	chr12:21035600-21036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:21035600-21036600	Enhancers	Rectal Smooth Muscle	rectum
42	chr12:21035600-21037800	Enhancers	Colon Smooth Muscle	Colon
43	chr12:21035800-21036600	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr12:21035800-21037000	Enhancers	Adipose Nuclei	Adipose
45	chr12:21035800-21037600	Enhancers	HUVEC	blood vessel
46	chr12:21035800-21038200	Enhancers	A549	lung
47	chr12:21038200-21038400	Flanking Active TSS	A549	lung
48	chr12:21038400-21038800	Enhancers	A549	lung
49	chr12:21038800-21040600	Weak transcription	A549	lung
50	chr12:21039000-21040000	Strong transcription	Liver	Liver

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