Variant report

Variant	esv1815052
Chromosome Location	chr12:31230871-31350602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1028)
CpG islands
(count:1099)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1028 , 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	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
2	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
5	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
6	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
7	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
8	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
9	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
16	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
17	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
19	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
20	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
21	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
22	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
24	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
25	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr12:31271974-31272145	GM12878	blood:	n/a	n/a
27	CHD2	chr12:31270194-31270459	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr12:31270114-31270314	GM12878	blood:	n/a	n/a
30	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
31	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a
32	CTBP2	chr12:31270123-31270826	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr12:31271446-31272443	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr12:31270100-31270250	NB4	blood:	n/a	n/a
35	CTCF	chr12:31330536-31330757	HUVEC	blood vessel:	n/a	chr12:31330654-31330675
36	CTCF	chr12:31322167-31322212	Medullo	brain:	n/a	n/a
37	CTCF	chr12:31253627-31253667	GM10248	blood:	n/a	n/a
38	CTCF	chr12:31330500-31330650	RPTEC	kidney:	n/a	n/a
39	CTCF	chr12:31304422-31304546	NHEK	skin:	n/a	n/a
40	CTCF	chr12:31270120-31270270	GM12872	blood:	n/a	n/a
41	CTCF	chr12:31330538-31330742	HepG2	liver:	n/a	chr12:31330654-31330675
42	CTCF	chr12:31270067-31270345	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:31255738-31255746	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr12:31270120-31270270	Caco-2	colon:	n/a	n/a
45	CTCF	chr12:31304489-31304579	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr12:31270660-31270810	AG04449	skin:	n/a	n/a
47	CTCF	chr12:31270100-31270250	GM12873	blood:	n/a	n/a
48	CTCF	chr12:31230850-31231305	A549	lung:	n/a	chr12:31231120-31231136
49	CTCF	chr12:31304382-31304560	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:31330617-31330771	NHEK	skin:	n/a	chr12:31330654-31330675

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31272119-31272169	HRCEpiC	kidney:	n/a
2	chr12:31272119-31272169	HRCEpiC	kidney:	n/a
3	chr12:31255279-31255329	SK-N-MC	brain:	n/a
4	chr12:31254007-31254057	HIPEpiC	eye:	n/a
5	chr12:31257362-31257412	PFSK-1	brain:	n/a
6	chr12:31272865-31272915	GM12892	blood:	n/a
7	chr12:31274424-31274474	NB4	blood:	n/a
8	chr12:31272112-31272162	Hepatocyte	liver:	n/a
9	chr12:31257362-31257412	AG09309	skin:	n/a
10	chr12:31254036-31254086	MCF-7	breast:	n/a
11	chr12:31316348-31316398	SK-N-SH_RA	brain:	n/a
12	chr12:31255279-31255329	HCF	heart:	n/a
13	chr12:31256838-31256888	HRPEpiC	eye:	n/a
14	chr12:31272112-31272162	GM19239	blood:	n/a
15	chr12:31274424-31274474	AG04449	skin:	fetal
16	chr12:31276852-31276902	NB4	blood:	n/a
17	chr12:31255279-31255329	HUVEC	blood vessel:	n/a
18	chr12:31256838-31256888	SK-N-SH	brain:	n/a
19	chr12:31257362-31257412	GM06990	blood:	n/a
20	chr12:31233201-31233251	GM06990	blood:	n/a
21	chr12:31257362-31257412	ECC-1	luminal epithelium:	n/a
22	chr12:31272112-31272162	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:31276852-31276902	BJ	skin:	n/a
24	chr12:31230936-31230986	HCM	heart:	n/a
25	chr12:31276852-31276902	PANC-1	pancreas:	n/a
26	chr12:31241496-31241546	Hepatocyte	liver:	n/a
27	chr12:31272114-31272164	SK-N-SH	brain:	n/a
28	chr12:31270326-31270376	SAEC	small airway:	n/a
29	chr12:31254036-31254086	SAEC	small airway:	n/a
30	chr12:31316348-31316398	GM06990	blood:	n/a
31	chr12:31256838-31256888	HL-60	blood:	n/a
32	chr12:31272114-31272164	HRCEpiC	kidney:	n/a
33	chr12:31272865-31272915	GM12878	blood:	n/a
34	chr12:31271429-31271479	K562	blood:	n/a
35	chr12:31272119-31272169	Hela-S3	cervix:	n/a
36	chr12:31230936-31230986	HRPEpiC	eye:	n/a
37	chr12:31254007-31254057	GM12878	blood:	n/a
38	chr12:31271429-31271479	HMEC	breast:	n/a
39	chr12:31255279-31255329	HRPEpiC	eye:	n/a
40	chr12:31272119-31272169	HEK293	kidney:	embryo
41	chr12:31254007-31254057	Jurkat	blood:	n/a
42	chr12:31257362-31257412	HEK293	kidney:	embryo
43	chr12:31241496-31241546	AG10803	skin:	n/a
44	chr12:31230936-31230986	AG04449	skin:	fetal
45	chr12:31254036-31254086	GM12892	blood:	n/a
46	chr12:31272112-31272162	ProgFib	skin:	n/a
47	chr12:31230936-31230986	NHBE	bronchial:	n/a
48	chr12:31272865-31272915	T-47D	breast:	n/a
49	chr12:31272114-31272164	HMEC	breast:	n/a
50	chr12:31254007-31254057	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
2	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
2	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
3	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
4	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
5	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000177359	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000177359	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
DDX11	CpG island
ENSG00000243517	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000245614	chromatin interactions

Extended variants
information (count: 3013 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3013 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189954342	chr12:31230890-31230891	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs567535304	chr12:31230911-31230912	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs538063323	chr12:31230921-31230922	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs2553163	chr12:31230967-31230968	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
5	rs556375065	chr12:31230981-31230982	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
6	rs574858482	chr12:31230990-31230991	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs2553162	chr12:31231000-31231001	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
8	rs377251768	chr12:31231016-31231017	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs544767973	chr12:31231047-31231048	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs2553161	chr12:31231049-31231050	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs553778176	chr12:31231114-31231115	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs77842499	chr12:31231138-31231139	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs542177518	chr12:31231152-31231153	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
14	rs1811284	chr12:31231158-31231159	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
15	rs562066003	chr12:31231164-31231165	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
16	rs4031358	chr12:31231167-31231168	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
17	rs147639058	chr12:31231210-31231211	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs2553159	chr12:31231227-31231228	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
19	rs7299908	chr12:31231230-31231231	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562931663	chr12:31231297-31231298	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
21	rs533511750	chr12:31231350-31231351	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
22	rs551585416	chr12:31231351-31231352	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
23	rs566914559	chr12:31231352-31231353	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
24	rs527700858	chr12:31231353-31231354	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
25	rs150002506	chr12:31231366-31231367	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs376585013	chr12:31231375-31231376	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
27	rs145236589	chr12:31231417-31231418	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
28	rs368329103	chr12:31231420-31231421	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs199851675	chr12:31231421-31231422	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
30	rs538124837	chr12:31231548-31231549	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs549992304	chr12:31231594-31231595	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs571350792	chr12:31231603-31231604	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs34895155	chr12:31231604-31231605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35973448	chr12:31231623-31231624	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs201391476	chr12:31231640-31231641	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs371159957	chr12:31231685-31231686	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs553596338	chr12:31231691-31231692	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs572074551	chr12:31231712-31231713	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs576202052	chr12:31231722-31231723	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs575720824	chr12:31231726-31231727	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs535870816	chr12:31231736-31231737	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs554126950	chr12:31231782-31231783	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs574034865	chr12:31231783-31231784	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs544497950	chr12:31231801-31231802	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs563148798	chr12:31231809-31231810	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs578115855	chr12:31231832-31231833	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs545546856	chr12:31231846-31231847	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs138681717	chr12:31231861-31231862	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs543457415	chr12:31231868-31231869	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs527766081	chr12:31231883-31231884	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227600-31235600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:31227600-31235800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:31227600-31236800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:31227600-31237000	Weak transcription	Aorta	Aorta
5	chr12:31227800-31232400	Weak transcription	Spleen	Spleen
6	chr12:31227800-31232800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:31227800-31233600	Weak transcription	Fetal Intestine Large	intestine
8	chr12:31227800-31234000	Weak transcription	Esophagus	oesophagus
9	chr12:31227800-31235600	Weak transcription	Primary B cells from cord blood	blood
10	chr12:31227800-31235600	Weak transcription	Fetal Intestine Small	intestine
11	chr12:31227800-31235800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:31227800-31236000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr12:31227800-31236800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr12:31227800-31236800	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:31227800-31237000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:31227800-31237000	Weak transcription	Gastric	stomach
17	chr12:31227800-31237000	Weak transcription	Lung	lung
18	chr12:31227800-31237000	Weak transcription	Right Ventricle	heart
19	chr12:31227800-31237400	Weak transcription	Ovary	ovary
20	chr12:31227800-31240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:31227800-31242000	Weak transcription	Left Ventricle	heart
22	chr12:31227800-31242600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
24	chr12:31228000-31231000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:31228000-31231000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:31228000-31231200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr12:31228000-31231400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr12:31228000-31232400	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr12:31228000-31232400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:31228000-31232800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:31228000-31232800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr12:31228000-31232800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr12:31228000-31233000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:31228000-31233000	Weak transcription	NHEK	skin
35	chr12:31228000-31233600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr12:31228000-31233600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr12:31228000-31233800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr12:31228000-31233800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr12:31228000-31234000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr12:31228000-31234200	Weak transcription	Fetal Muscle Leg	muscle
41	chr12:31228000-31235200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr12:31228000-31235600	Weak transcription	Thymus	Thymus
43	chr12:31228000-31235800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:31228000-31235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:31228000-31235800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:31228000-31235800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:31228000-31235800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr12:31228000-31236000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr12:31228000-31236200	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr12:31228000-31236600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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