Variant report

Variant	nsv559559
Chromosome Location	chr12:83505512-83765069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:853)
CpG islands
(count:244)
Chromatin interactive
region (count:74)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83659589-83659838	K562	blood:	n/a	n/a
2	ARID3A	chr12:83543919-83544914	K562	blood:	n/a	n/a
3	ARID3A	chr12:83590280-83591022	K562	blood:	n/a	n/a
4	ARID3A	chr12:83566082-83567580	K562	blood:	n/a	n/a
5	ARID3A	chr12:83568375-83568709	K562	blood:	n/a	n/a
6	ARID3A	chr12:83729583-83729955	K562	blood:	n/a	n/a
7	ATF1	chr12:83566939-83567378	K562	blood:	n/a	n/a
8	ATF1	chr12:83729611-83729797	K562	blood:	n/a	n/a
9	ATF1	chr12:83707708-83707911	K562	blood:	n/a	n/a
10	ATF1	chr12:83590456-83590832	K562	blood:	n/a	n/a
11	ATF1	chr12:83515598-83515687	K562	blood:	n/a	n/a
12	ATF1	chr12:83547302-83547439	K562	blood:	n/a	n/a
13	ATF3	chr12:83566990-83567362	K562	blood:	n/a	n/a
14	ATF3	chr12:83522349-83522607	K562	blood:	n/a	n/a
15	BACH1	chr12:83567817-83568066	K562	blood:	n/a	n/a
16	BACH1	chr12:83551046-83551105	K562	blood:	n/a	n/a
17	BACH1	chr12:83525983-83526025	K562	blood:	n/a	n/a
18	BATF	chr12:83546930-83547226	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:83544132-83544573	K562	blood:	n/a	n/a
20	BCLAF1	chr12:83566983-83567445	K562	blood:	n/a	n/a
21	BCLAF1	chr12:83544125-83544611	K562	blood:	n/a	n/a
22	BHLHE40	chr12:83706864-83706881	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:83617845-83618204	K562	blood:	n/a	n/a
24	BHLHE40	chr12:83566786-83567433	K562	blood:	n/a	n/a
25	BHLHE40	chr12:83590479-83590519	K562	blood:	n/a	n/a
26	CBX3	chr12:83566957-83567421	K562	blood:	n/a	n/a
27	CBX3	chr12:83594804-83595136	K562	blood:	n/a	n/a
28	CBX3	chr12:83700713-83700956	K562	blood:	n/a	n/a
29	CBX3	chr12:83585557-83585905	K562	blood:	n/a	n/a
30	CBX3	chr12:83533601-83533957	K562	blood:	n/a	n/a
31	CBX3	chr12:83511788-83512089	K562	blood:	n/a	n/a
32	CBX3	chr12:83590437-83590926	K562	blood:	n/a	n/a
33	CCNT2	chr12:83567614-83568154	K562	blood:	n/a	n/a
34	CCNT2	chr12:83544274-83544770	K562	blood:	n/a	n/a
35	CCNT2	chr12:83566983-83567388	K562	blood:	n/a	n/a
36	CCNT2	chr12:83590406-83590814	K562	blood:	n/a	n/a
37	CCNT2	chr12:83707716-83707963	K562	blood:	n/a	chr12:83707897-83707917 chr12:83707763-83707783
38	CCNT2	chr12:83729614-83729843	K562	blood:	n/a	n/a
39	CEBPB	chr12:83593675-83593940	HepG2	liver:	n/a	chr12:83593848-83593859 chr12:83593798-83593811 chr12:83593798-83593809 chr12:83593799-83593810
40	CEBPB	chr12:83590780-83591064	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:83746433-83746741	K562	blood:	n/a	chr12:83746570-83746581 chr12:83746570-83746583 chr12:83746570-83746583
42	CEBPB	chr12:83590482-83591067	K562	blood:	n/a	n/a
43	CEBPB	chr12:83700564-83700819	HepG2	liver:	n/a	chr12:83700688-83700699
44	CEBPB	chr12:83556948-83557295	K562	blood:	n/a	chr12:83557124-83557133 chr12:83557122-83557135 chr12:83557124-83557135
45	CEBPB	chr12:83584443-83585129	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:83522391-83522642	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr12:83544488-83544736	K562	blood:	n/a	n/a
48	CEBPB	chr12:83584766-83585081	K562	blood:	n/a	n/a
49	CEBPB	chr12:83566263-83566543	K562	blood:	n/a	n/a
50	CEBPB	chr12:83584538-83585156	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83592588-83592638	AG09309	skin:	n/a
2	chr12:83744367-83744417	NB4	blood:	n/a
3	chr12:83591371-83591421	ProgFib	skin:	n/a
4	chr12:83744367-83744417	HMEC	breast:	n/a
5	chr12:83591371-83591421	MCF10A-Er-Src	breast:	n/a
6	chr12:83595509-83595559	SK-N-MC	brain:	n/a
7	chr12:83592588-83592638	PFSK-1	brain:	n/a
8	chr12:83595509-83595559	SKMC	muscle:	n/a
9	chr12:83595509-83595559	HIPEpiC	eye:	n/a
10	chr12:83591371-83591421	HCPEpiC	choroid plexus:	n/a
11	chr12:83591371-83591421	HNPCEpiC	eye:	n/a
12	chr12:83595509-83595559	AG09319	gingival:	n/a
13	chr12:83595509-83595559	SAEC	small airway:	n/a
14	chr12:83744367-83744417	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:83592588-83592638	HepG2	liver:	n/a
16	chr12:83595509-83595559	HCT-116	colon:	n/a
17	chr12:83592588-83592638	CMK	blood:	n/a
18	chr12:83744367-83744417	PFSK-1	brain:	n/a
19	chr12:83591371-83591421	BE2_C	brain:	n/a
20	chr12:83744367-83744417	HNPCEpiC	eye:	n/a
21	chr12:83744367-83744417	HEK293	kidney:	embryo
22	chr12:83592588-83592638	HMEC	breast:	n/a
23	chr12:83744367-83744417	SK-N-SH_RA	brain:	n/a
24	chr12:83595509-83595559	LNCaP	prostate:	n/a
25	chr12:83592588-83592638	GM12892	blood:	n/a
26	chr12:83591371-83591421	HMEC	breast:	n/a
27	chr12:83592588-83592638	GM19239	blood:	n/a
28	chr12:83744367-83744417	HRE	kidney:	n/a
29	chr12:83591371-83591421	GM12892	blood:	n/a
30	chr12:83591371-83591421	Hela-S3	cervix:	n/a
31	chr12:83595509-83595559	PrEC	prostate:	n/a
32	chr12:83591371-83591421	HIPEpiC	eye:	n/a
33	chr12:83592588-83592638	GM06990	blood:	n/a
34	chr12:83744367-83744417	U87	brain:	n/a
35	chr12:83744367-83744417	IMR90	lung:	fetal
36	chr12:83744367-83744417	HRCEpiC	kidney:	n/a
37	chr12:83591371-83591421	NB4	blood:	n/a
38	chr12:83744367-83744417	PrEC	prostate:	n/a
39	chr12:83592588-83592638	GM12891	blood:	n/a
40	chr12:83591371-83591421	SAEC	small airway:	n/a
41	chr12:83595509-83595559	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:83592588-83592638	NT2-D1	testis:	n/a
43	chr12:83591371-83591421	HEEpiC	esophagus:	n/a
44	chr12:83595509-83595559	IMR90	lung:	fetal
45	chr12:83591371-83591421	BJ	skin:	n/a
46	chr12:83744367-83744417	AG09309	skin:	n/a
47	chr12:83592588-83592638	HCM	heart:	n/a
48	chr12:83591371-83591421	HUVEC	blood vessel:	n/a
49	chr12:83592588-83592638	HCPEpiC	choroid plexus:	n/a
50	chr12:83591371-83591421	NH-A	brain:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:83567059..83568732-chr12:83568877..83572188,3	K562	blood:
2	chr12:83594175..83596162-chr12:83607861..83610318,2	K562	blood:
3	chr12:83525944..83528624-chr12:83539787..83542327,2	K562	blood:
4	chr12:83721451..83723173-chr12:83727396..83729425,2	K562	blood:
5	chr12:83650313..83652424-chr12:83654399..83655919,2	K562	blood:
6	chr12:83750288..83752818-chr12:83758244..83760757,2	K562	blood:
7	chr12:83531363..83533075-chr12:83548152..83550320,2	K562	blood:
8	chr12:83559777..83562600-chr12:83582950..83585576,2	K562	blood:
9	chr12:83584738..83586685-chr12:83587264..83589926,2	K562	blood:
10	chr12:83584738..83586685-chr12:83587264..83589926,2	K562	blood:
11	chr12:83734504..83737093-chr12:83742802..83744380,2	K562	blood:
12	chr12:83569275..83573489-chr12:83574192..83577133,4	K562	blood:
13	chr12:83572167..83574057-chr12:83581000..83582691,2	K562	blood:
14	chr12:83516860..83518409-chr12:83518593..83521378,2	MCF-7	breast:
15	chr12:83549123..83550783-chr12:83557116..83558963,2	K562	blood:
16	chr12:83511831..83514804-chr12:83521599..83524454,2	K562	blood:
17	chr12:83542565..83545008-chr12:83566532..83568731,2	K562	blood:
18	chr12:83516860..83518409-chr12:83518593..83521378,2	MCF-7	breast:
19	chr12:83535330..83537373-chr12:83539201..83541906,2	MCF-7	breast:
20	chr12:83551485..83553792-chr12:83556575..83559137,3	K562	blood:
21	chr12:83592254..83594970-chr12:83596258..83598590,2	K562	blood:
22	chr12:83551485..83553792-chr12:83556575..83559137,3	K562	blood:
23	chr12:83521701..83523329-chr12:83525672..83527174,2	K562	blood:
24	chr12:83543290..83546806-chr12:83549087..83551687,3	K562	blood:
25	chr12:83702212..83704264-chr12:83726364..83728479,2	MCF-7	breast:
26	chr12:83544204..83547300-chr12:83565294..83568288,4	K562	blood:
27	chr12:83559514..83561269-chr12:83566076..83567832,2	K562	blood:
28	chr12:83713152..83715052-chr12:83721366..83724257,2	MCF-7	breast:
29	chr12:83713152..83715052-chr12:83721366..83724257,2	MCF-7	breast:
30	chr12:83542565..83545008-chr12:83566532..83568731,2	K562	blood:
31	chr12:83485429..83487033-chr12:83528261..83531260,2	K562	blood:
32	chr12:83734504..83737093-chr12:83742802..83744380,2	K562	blood:
33	chr12:83721451..83723173-chr12:83727396..83729425,2	K562	blood:
34	chr12:83569275..83573489-chr12:83574192..83577133,4	K562	blood:
35	chr12:83572167..83574057-chr12:83581000..83582691,2	K562	blood:
36	chr12:83702212..83704264-chr12:83726364..83728479,2	MCF-7	breast:
37	chr12:83543034..83546806-chr12:83548312..83551212,4	K562	blood:
38	chr12:83621899..83623681-chr12:83628874..83631467,2	MCF-7	breast:
39	chr12:83594175..83596162-chr12:83607861..83610318,2	K562	blood:
40	chr12:83538640..83540681-chr12:83564566..83567438,2	K562	blood:
41	chr12:83563184..83563801-chr7:95030189..95031002,2	MCF-7	breast:
42	chr12:83559777..83562600-chr12:83582950..83585576,2	K562	blood:
43	chr12:83578114..83580861-chr12:83582749..83585720,2	K562	blood:
44	chr12:83567163..83569617-chr12:83571861..83573783,2	K562	blood:
45	chr12:83561874..83563681-chr12:83576352..83578180,2	MCF-7	breast:
46	chr12:83531135..83533652-chr12:83540992..83544898,3	K562	blood:
47	chr12:83511831..83514804-chr12:83521599..83524454,2	K562	blood:
48	chr12:83544204..83547300-chr12:83565294..83568288,4	K562	blood:
49	chr12:83554178..83558024-chr12:83564818..83567796,3	K562	blood:
50	chr12:83500913..83502581-chr12:83513715..83516679,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMTC2-1	chr12:83565369-83565455	ENSG00000258338
2	lnc-TMTC2-1	chr12:83565865-83566519	ENSG00000258338

No data

Variant related genes	Relation type
ENSG00000258338	TF binding region
RPL6P25	TF binding region
ENSG00000258338	CpG island
RPL6P25	CpG island
ENSG00000258338	chromatin interactions
ENSG00000213270	chromatin interactions
ENSG00000149923	chromatin interactions

Extended variants
information (count: 4758 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4758 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs962573	chr12:83505512-83505513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189159817	chr12:83505559-83505560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545526497	chr12:83505588-83505589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180842343	chr12:83505627-83505628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556411322	chr12:83505628-83505629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75699032	chr12:83505635-83505636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185837381	chr12:83505708-83505709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1356443	chr12:83505716-83505717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371253481	chr12:83505724-83505725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189902970	chr12:83505730-83505731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572166535	chr12:83505737-83505738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551062658	chr12:83505759-83505760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562888943	chr12:83505780-83505781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181221238	chr12:83505788-83505789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187080002	chr12:83505793-83505794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144335344	chr12:83505834-83505835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1210961	chr12:83505858-83505859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551519289	chr12:83505876-83505877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566852747	chr12:83505884-83505885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146605656	chr12:83505902-83505903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377254035	chr12:83505911-83505912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568273759	chr12:83505925-83505926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554317528	chr12:83505937-83505938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572251076	chr12:83505948-83505949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73135823	chr12:83505961-83505962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534797914	chr12:83506014-83506015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568898058	chr12:83506072-83506073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145153946	chr12:83506082-83506083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374196022	chr12:83506100-83506101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75216223	chr12:83506102-83506103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572477049	chr12:83506168-83506169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190624958	chr12:83506205-83506206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564758588	chr12:83506298-83506299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114270673	chr12:83506339-83506340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79276574	chr12:83506345-83506346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145848008	chr12:83506349-83506350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574273891	chr12:83506357-83506358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78790403	chr12:83506417-83506418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115847569	chr12:83506445-83506446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116386261	chr12:83506447-83506448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545459117	chr12:83506449-83506450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560495005	chr12:83506492-83506493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527647257	chr12:83506535-83506536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546921679	chr12:83506566-83506567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568409191	chr12:83506579-83506580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529177521	chr12:83506592-83506593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550533050	chr12:83506605-83506606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569009264	chr12:83506666-83506667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79842806	chr12:83506668-83506669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557396425	chr12:83506673-83506674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	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
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83469000-83507600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:83476800-83507200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:83492600-83507800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:83492600-83515800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr12:83496400-83509000	Weak transcription	Fetal Lung	lung
6	chr12:83498800-83507600	Weak transcription	Brain Anterior Caudate	brain
7	chr12:83499600-83507800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:83500000-83515200	Weak transcription	Brain Substantia Nigra	brain
9	chr12:83502400-83515600	Weak transcription	Fetal Stomach	stomach
10	chr12:83503600-83507800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:83503600-83515800	Weak transcription	Fetal Brain Male	brain
12	chr12:83506200-83506400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr12:83506400-83506600	Enhancers	Brain Angular Gyrus	brain
14	chr12:83506400-83507400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr12:83506600-83507400	Weak transcription	Brain Angular Gyrus	brain
16	chr12:83507200-83508000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:83507200-83508000	Enhancers	Brain Hippocampus Middle	brain
18	chr12:83507200-83508200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:83507400-83507600	Enhancers	Brain Angular Gyrus	brain
20	chr12:83507400-83508200	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr12:83507400-83508200	Enhancers	Fetal Muscle Leg	muscle
22	chr12:83507600-83507800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:83507600-83507800	Enhancers	Brain Anterior Caudate	brain
24	chr12:83507600-83508400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:83507800-83508000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:83507800-83508200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:83507800-83508400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:83507800-83515400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:83508000-83508200	Enhancers	Fetal Brain Female	brain
30	chr12:83508000-83511200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:83508200-83513400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:83508800-83509000	Enhancers	Fetal Brain Female	brain
33	chr12:83509000-83509200	Enhancers	Fetal Lung	lung
34	chr12:83509200-83509600	Weak transcription	Fetal Lung	lung
35	chr12:83515000-83515800	Enhancers	Brain Angular Gyrus	brain
36	chr12:83515000-83515800	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr12:83515200-83515600	Enhancers	Brain Cingulate Gyrus	brain
38	chr12:83515200-83515600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:83515200-83515800	Enhancers	Brain Hippocampus Middle	brain
40	chr12:83515200-83515800	Enhancers	Brain Substantia Nigra	brain
41	chr12:83515200-83516000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:83515200-83516200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:83515400-83515800	Enhancers	Brain Anterior Caudate	brain
44	chr12:83515400-83516200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:83515400-83516600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:83515400-83516600	Enhancers	K562	blood
47	chr12:83515600-83516200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr12:83515600-83516400	Genic enhancers	Fetal Stomach	stomach
49	chr12:83515600-83516800	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr12:83515800-83516000	ZNF genes & repeats	Fetal Intestine Small	intestine

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