Variant report

Variant	nsv515735
Chromosome Location	chr12:21010048-21420712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:367)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1415 , 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	chr12:21380331-21380521	K562	blood:	n/a	n/a
4	BACH1	chr12:21322799-21322999	K562	blood:	n/a	n/a
5	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	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	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr12:21103222-21103500	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:21233354-21233510	A549	lung:	n/a	n/a
14	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
15	CEBPB	chr12:21418941-21419217	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:21168771-21169100	A549	lung:	n/a	chr12:21168919-21168930
17	CEBPB	chr12:21168858-21169067	H1-hESC	embryonic stem cell:	n/a	chr12:21168919-21168930
18	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
19	CEBPB	chr12:21356602-21356832	H1-hESC	embryonic stem cell:	n/a	chr12:21356695-21356706
20	CEBPB	chr12:21356582-21356854	A549	lung:	n/a	chr12:21356695-21356706
21	CEBPB	chr12:21175943-21176096	H1-hESC	embryonic stem cell:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
22	CEBPB	chr12:21409557-21409626	K562	blood:	n/a	chr12:21409600-21409611
23	CEBPB	chr12:21127431-21127656	HepG2	liver:	n/a	chr12:21127518-21127529
24	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
25	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
26	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
27	CEBPB	chr12:21175930-21176170	HepG2	liver:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
28	CEBPB	chr12:21260027-21260258	HepG2	liver:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
29	CEBPB	chr12:21234009-21234357	HepG2	liver:	n/a	chr12:21234179-21234190
30	CEBPB	chr12:21193579-21193868	A549	lung:	n/a	chr12:21193754-21193765
31	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
32	CEBPB	chr12:21417548-21417736	H1-hESC	embryonic stem cell:	n/a	chr12:21417620-21417631
33	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
34	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
35	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
36	CEBPB	chr12:21417501-21417806	IMR90	lung:	n/a	chr12:21417620-21417631
37	CEBPB	chr12:21260031-21260260	IMR90	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
38	CEBPB	chr12:21394753-21395095	HepG2	liver:	n/a	chr12:21394924-21394935
39	CEBPB	chr12:21356519-21356864	IMR90	lung:	n/a	chr12:21356695-21356706
40	CEBPB	chr12:21417474-21417800	A549	lung:	n/a	chr12:21417620-21417631
41	CEBPB	chr12:21193722-21193901	H1-hESC	embryonic stem cell:	n/a	chr12:21193754-21193765
42	CEBPB	chr12:21260029-21260209	A549	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
43	CEBPB	chr12:21356579-21356809	HepG2	liver:	n/a	chr12:21356695-21356706
44	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
45	CEBPB	chr12:21410877-21411098	A549	lung:	n/a	n/a
46	CEBPB	chr12:21234048-21234229	H1-hESC	embryonic stem cell:	n/a	chr12:21234179-21234190
47	CEBPB	chr12:21417491-21417780	HepG2	liver:	n/a	chr12:21417620-21417631
48	CEBPB	chr12:21133477-21133530	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:21243024-21243307	HepG2	liver:	n/a	chr12:21243166-21243177
50	CEBPB	chr12:21409453-21409717	HepG2	liver:	n/a	chr12:21409600-21409611

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21324585-21324635	CMK	blood:	n/a
2	chr12:21324585-21324635	CMK	blood:	n/a
3	chr12:21418929-21418979	HRPEpiC	eye:	n/a
4	chr12:21287375-21287425	U87	brain:	n/a
5	chr12:21324585-21324635	GM06990	blood:	n/a
6	chr12:21287375-21287425	HMEC	breast:	n/a
7	chr12:21283725-21283775	NH-A	brain:	n/a
8	chr12:21324585-21324635	AG09319	gingival:	n/a
9	chr12:21015340-21015390	MCF10A-Er-Src	breast:	n/a
10	chr12:21015340-21015390	AG04449	skin:	fetal
11	chr12:21324585-21324635	PFSK-1	brain:	n/a
12	chr12:21014317-21014367	Caco-2	colon:	n/a
13	chr12:21015340-21015390	GM12892	blood:	n/a
14	chr12:21283725-21283775	K562	blood:	n/a
15	chr12:21418929-21418979	HCPEpiC	choroid plexus:	n/a
16	chr12:21418929-21418979	H1-hESC	embryonic stem cell:	embryo
17	chr12:21287375-21287425	SK-N-MC	brain:	n/a
18	chr12:21014317-21014367	HNPCEpiC	eye:	n/a
19	chr12:21287375-21287425	AoSMC	blood vessel:	n/a
20	chr12:21324585-21324635	GM12892	blood:	n/a
21	chr12:21418929-21418979	AG10803	skin:	n/a
22	chr12:21015340-21015390	AG10803	skin:	n/a
23	chr12:21015340-21015390	NT2-D1	testis:	n/a
24	chr12:21015340-21015390	NB4	blood:	n/a
25	chr12:21287375-21287425	ovcar-3	ovarian:	n/a
26	chr12:21014317-21014367	H1-hESC	embryonic stem cell:	embryo
27	chr12:21015340-21015390	T-47D	breast:	n/a
28	chr12:21418929-21418979	HRE	kidney:	n/a
29	chr12:21014317-21014367	Hepatocyte	liver:	n/a
30	chr12:21014317-21014367	NT2-D1	testis:	n/a
31	chr12:21015340-21015390	HMEC	breast:	n/a
32	chr12:21287375-21287425	HCF	heart:	n/a
33	chr12:21418929-21418979	BE2_C	brain:	n/a
34	chr12:21418929-21418979	HAEpiC	amniotic membrane:	n/a
35	chr12:21014317-21014367	HAEpiC	amniotic membrane:	n/a
36	chr12:21287375-21287425	BJ	skin:	n/a
37	chr12:21287375-21287425	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:21015340-21015390	LNCaP	prostate:	n/a
39	chr12:21324585-21324635	NHDF-neo	bronchial:	n/a
40	chr12:21324585-21324635	NHBE	bronchial:	n/a
41	chr12:21015340-21015390	BE2_C	brain:	n/a
42	chr12:21283725-21283775	T-47D	breast:	n/a
43	chr12:21324585-21324635	IMR90	lung:	fetal
44	chr12:21418929-21418979	HNPCEpiC	eye:	n/a
45	chr12:21324585-21324635	GM12878	blood:	n/a
46	chr12:21283725-21283775	ProgFib	skin:	n/a
47	chr12:21015340-21015390	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:21287375-21287425	NB4	blood:	n/a
49	chr12:21418929-21418979	HEEpiC	esophagus:	n/a
50	chr12:21287375-21287425	Caco-2	colon:	n/a

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

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

(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
ENSG00000257062	TF binding region
SLCO1B1	TF binding region
SLCO1B7	TF binding region
SLCO1B3	TF binding region
ENSG00000257062	CpG island
SLCO1B1	CpG island
SLCO1B7	CpG island
SLCO1B3	CpG island

Extended variants
information (count: 13006 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:13006 , 50 per page) page: 1 2 3 4 5 6 7 ... 261

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2900474	chr12:21010048-21010049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7311387	chr12:21010085-21010086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs370371175	chr12:21010098-21010099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184625812	chr12:21010099-21010100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533963157	chr12:21010107-21010108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554667625	chr12:21010135-21010136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574734836	chr12:21010147-21010148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542571086	chr12:21010167-21010168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148020867	chr12:21010175-21010176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559656457	chr12:21010181-21010182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369362633	chr12:21010194-21010195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573150638	chr12:21010219-21010220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371260970	chr12:21010232-21010233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7297444	chr12:21010297-21010298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs565072688	chr12:21010333-21010334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7312103	chr12:21010371-21010372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs200823453	chr12:21010403-21010404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149348597	chr12:21010483-21010484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189091786	chr12:21010504-21010505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529665684	chr12:21010543-21010544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546168465	chr12:21010549-21010550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200644037	chr12:21010571-21010572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181849458	chr12:21010580-21010581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146310477	chr12:21010604-21010605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565435458	chr12:21010662-21010663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4149111	chr12:21010671-21010672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184781776	chr12:21010722-21010723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537960940	chr12:21010753-21010754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4149112	chr12:21010782-21010783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561737715	chr12:21010794-21010795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568382584	chr12:21010797-21010798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369625511	chr12:21010851-21010852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554189356	chr12:21010853-21010854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4149113	chr12:21010856-21010857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530246219	chr12:21010915-21010916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545279740	chr12:21010952-21010953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201395594	chr12:21010954-21010955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558798281	chr12:21010958-21010959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77390746	chr12:21010963-21010964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114546482	chr12:21010978-21010979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543999704	chr12:21010992-21010993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532767114	chr12:21011023-21011024	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561067709	chr12:21011042-21011043	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374262379	chr12:21011056-21011057	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142322493	chr12:21011113-21011114	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140759897	chr12:21011158-21011159	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11831951	chr12:21011179-21011180	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57712877	chr12:21011208-21011209	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59976661	chr12:21011209-21011210	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144607206	chr12:21011210-21011211	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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	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:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21006200-21011000	Weak transcription	Liver	Liver
2	chr12:21006600-21018000	Weak transcription	A549	lung
3	chr12:21011000-21014600	Strong transcription	Liver	Liver
4	chr12:21014600-21015400	Weak transcription	Liver	Liver
5	chr12:21015400-21018400	Strong transcription	Liver	Liver
6	chr12:21017800-21019200	Enhancers	HUVEC	blood vessel
7	chr12:21018000-21018200	Strong transcription	A549	lung
8	chr12:21018200-21018800	Weak transcription	A549	lung
9	chr12:21018400-21020800	Weak transcription	Liver	Liver
10	chr12:21018800-21020600	Strong transcription	A549	lung
11	chr12:21019800-21020000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:21020000-21020400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:21020000-21020600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:21020600-21021600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:21020600-21027400	Weak transcription	A549	lung
16	chr12:21020800-21021200	Strong transcription	Liver	Liver
17	chr12:21020800-21021600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:21021200-21024600	Weak transcription	Liver	Liver
19	chr12:21021600-21022200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:21024600-21026200	Strong transcription	Liver	Liver
21	chr12:21026200-21027800	Weak transcription	Liver	Liver
22	chr12:21027400-21028400	Strong transcription	A549	lung
23	chr12:21027800-21029600	Strong transcription	Liver	Liver
24	chr12:21028400-21035800	Weak transcription	A549	lung
25	chr12:21029600-21032400	Weak transcription	Liver	Liver
26	chr12:21032400-21035400	Strong transcription	Liver	Liver
27	chr12:21034000-21034200	Enhancers	Rectal Smooth Muscle	rectum
28	chr12:21034400-21035000	Enhancers	Stomach Mucosa	stomach
29	chr12:21034400-21035600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:21035000-21035400	Weak transcription	Stomach Mucosa	stomach
31	chr12:21035400-21036000	Enhancers	Stomach Mucosa	stomach
32	chr12:21035400-21039000	Weak transcription	Liver	Liver
33	chr12:21035600-21036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:21035600-21036600	Enhancers	Rectal Smooth Muscle	rectum
35	chr12:21035600-21037800	Enhancers	Colon Smooth Muscle	Colon
36	chr12:21035800-21036600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr12:21035800-21037000	Enhancers	Adipose Nuclei	Adipose
38	chr12:21035800-21037600	Enhancers	HUVEC	blood vessel
39	chr12:21035800-21038200	Enhancers	A549	lung
40	chr12:21038200-21038400	Flanking Active TSS	A549	lung
41	chr12:21038400-21038800	Enhancers	A549	lung
42	chr12:21038800-21040600	Weak transcription	A549	lung
43	chr12:21039000-21040000	Strong transcription	Liver	Liver
44	chr12:21040000-21046600	Weak transcription	Liver	Liver
45	chr12:21044600-21054200	Weak transcription	A549	lung
46	chr12:21046600-21048400	Strong transcription	Liver	Liver
47	chr12:21048400-21052400	Weak transcription	Liver	Liver
48	chr12:21049800-21050200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:21051800-21052200	Weak transcription	Aorta	Aorta
50	chr12:21052400-21052600	Enhancers	Aorta	Aorta

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