Variant report

Variant	nsv973027
Chromosome Location	chr12:11173768-11184735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:489)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
2	CTCF	chr12:11178810-11178991	HepG2	liver:	n/a	n/a
3	CTCF	chr12:11178840-11178990	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr12:11178806-11179001	K562	blood:	n/a	n/a
5	CTCF	chr12:11178858-11178977	ProgFib	skin:	n/a	n/a
6	CTCF	chr12:11178820-11178970	HFF-Myc	foreskin:	n/a	n/a
7	CTCF	chr12:11178782-11179023	MCF-7	breast:	n/a	n/a
8	CTCF	chr12:11176040-11176190	BE2_C	brain:	n/a	n/a
9	CTCF	chr12:11178863-11178966	NHEK	skin:	n/a	n/a
10	CTCF	chr12:11178920-11179070	GM12868	blood:	n/a	n/a
11	CTCF	chr12:11178860-11179010	GM12872	blood:	n/a	n/a
12	CTCF	chr12:11178840-11178990	HEK293	kidney:	n/a	n/a
13	CTCF	chr12:11178880-11179030	A549	lung:	n/a	n/a
14	CTCF	chr12:11178820-11178970	GM12866	blood:	n/a	n/a
15	CTCF	chr12:11178760-11178910	GM12869	blood:	n/a	n/a
16	CTCF	chr12:11178880-11179030	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr12:11178800-11178950	AG09319	gingival:	n/a	n/a
18	CTCF	chr12:11178880-11179030	BJ	skin:	n/a	n/a
19	CTCF	chr12:11178780-11178930	WI-38	lung:	n/a	n/a
20	CTCF	chr12:11178820-11178970	NHEK	skin:	n/a	n/a
21	CTCF	chr12:11178840-11178990	GM12872	blood:	n/a	n/a
22	CTCF	chr12:11178820-11178970	HAc	cerebellar:	n/a	n/a
23	CTCF	chr12:11178800-11178950	GM12864	blood:	n/a	n/a
24	CTCF	chr12:11178840-11178990	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr12:11178800-11178950	HFF	foreskin:	n/a	n/a
26	CTCF	chr12:11178860-11179010	GM12871	blood:	n/a	n/a
27	CTCF	chr12:11178820-11178970	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11178860-11179010	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr12:11178795-11179005	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:11178820-11179007	K562	blood:	n/a	n/a
31	CTCF	chr12:11178840-11178990	HMF	breast:	n/a	n/a
32	CTCF	chr12:11178800-11178950	HMEC	breast:	n/a	n/a
33	CTCF	chr12:11178792-11179011	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:11178780-11178930	RPTEC	kidney:	n/a	n/a
35	CTCF	chr12:11178800-11178950	AG04450	lung:	n/a	n/a
36	CTCF	chr12:11178880-11179030	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:11178820-11178970	GM12873	blood:	n/a	n/a
38	CTCF	chr12:11178819-11178997	A549	lung:	n/a	n/a
39	CTCF	chr12:11178800-11178950	SAEC	small airway:	n/a	n/a
40	CTCF	chr12:11178800-11178950	HVMF	connective:	n/a	n/a
41	CTCF	chr12:11178700-11178990	HPF	lung:	n/a	n/a
42	CTCF	chr12:11178820-11178970	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr12:11178869-11178995	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:11178700-11178850	HCM	heart:	n/a	n/a
45	CTCF	chr12:11178840-11178990	A549	lung:	n/a	n/a
46	CTCF	chr12:11176080-11176230	HepG2	liver:	n/a	n/a
47	CTCF	chr12:11178700-11178850	K562	blood:	n/a	n/a
48	CTCF	chr12:11178880-11179030	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a
50	CTCF	chr12:11178785-11179055	MCF-7	breast:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11174898-11174948	PANC-1	pancreas:	n/a
2	chr12:11174898-11174948	PANC-1	pancreas:	n/a
3	chr12:11174898-11174948	LNCaP	prostate:	n/a
4	chr12:11176574-11176624	PFSK-1	brain:	n/a
5	chr12:11176386-11176436	AG04449	skin:	fetal
6	chr12:11176574-11176624	NB4	blood:	n/a
7	chr12:11176386-11176436	HCM	heart:	n/a
8	chr12:11176386-11176436	HCF	heart:	n/a
9	chr12:11184149-11184199	ovcar-3	ovarian:	n/a
10	chr12:11176386-11176436	SK-N-SH_RA	brain:	n/a
11	chr12:11184037-11184087	HRPEpiC	eye:	n/a
12	chr12:11174898-11174948	PFSK-1	brain:	n/a
13	chr12:11184149-11184199	BJ	skin:	n/a
14	chr12:11184149-11184199	SK-N-MC	brain:	n/a
15	chr12:11174898-11174948	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:11174898-11174948	Hepatocyte	liver:	n/a
17	chr12:11184037-11184087	HUVEC	blood vessel:	n/a
18	chr12:11184415-11184465	HAEpiC	amniotic membrane:	n/a
19	chr12:11184005-11184055	SK-N-SH_RA	brain:	n/a
20	chr12:11176386-11176436	Hepatocyte	liver:	n/a
21	chr12:11174898-11174948	HCT-116	colon:	n/a
22	chr12:11184037-11184087	HIPEpiC	eye:	n/a
23	chr12:11184149-11184199	HRCEpiC	kidney:	n/a
24	chr12:11176574-11176624	GM12891	blood:	n/a
25	chr12:11184415-11184465	T-47D	breast:	n/a
26	chr12:11176386-11176436	HPAEpiC	pulmonary alveolar:	n/a
27	chr12:11176386-11176436	AoSMC	blood vessel:	n/a
28	chr12:11174898-11174948	GM06990	blood:	n/a
29	chr12:11184005-11184055	A549	lung:	n/a
30	chr12:11184149-11184199	AoSMC	blood vessel:	n/a
31	chr12:11184415-11184465	AG04450	lung:	fetal
32	chr12:11184347-11184397	SK-N-SH	brain:	n/a
33	chr12:11176574-11176624	AoSMC	blood vessel:	n/a
34	chr12:11184149-11184199	HEEpiC	esophagus:	n/a
35	chr12:11184149-11184199	SK-N-SH	brain:	n/a
36	chr12:11184037-11184087	NB4	blood:	n/a
37	chr12:11176574-11176624	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:11184005-11184055	HUVEC	blood vessel:	n/a
39	chr12:11184149-11184199	AG09309	skin:	n/a
40	chr12:11184149-11184199	HUVEC	blood vessel:	n/a
41	chr12:11184347-11184397	HCT-116	colon:	n/a
42	chr12:11176386-11176436	HUVEC	blood vessel:	n/a
43	chr12:11174898-11174948	HCM	heart:	n/a
44	chr12:11184037-11184087	CMK	blood:	n/a
45	chr12:11174898-11174948	SK-N-MC	brain:	n/a
46	chr12:11184149-11184199	GM12891	blood:	n/a
47	chr12:11174898-11174948	HNPCEpiC	eye:	n/a
48	chr12:11176574-11176624	HUVEC	blood vessel:	n/a
49	chr12:11184149-11184199	K562	blood:	n/a
50	chr12:11184347-11184397	Hepatocyte	liver:	n/a

No data

Variant related genes	Relation type
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000268301	TF binding region
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000268301	CpG island

Extended variants
information (count: 710 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544698754	chr12:11173823-11173824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564860568	chr12:11173825-11173826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533463177	chr12:11173837-11173838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77147542	chr12:11173852-11173853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376115460	chr12:11173858-11173859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201628562	chr12:11173888-11173889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540478790	chr12:11173909-11173910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199968074	chr12:11173915-11173916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200684798	chr12:11173918-11173919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560410416	chr12:11173943-11173944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559736909	chr12:11173986-11173987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187963305	chr12:11173990-11173991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549148712	chr12:11173996-11173997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376578925	chr12:11174013-11174014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369341274	chr12:11174015-11174016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201855159	chr12:11174019-11174020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75874054	chr12:11174065-11174066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201011521	chr12:11174097-11174098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376992145	chr12:11174098-11174099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370493292	chr12:11174099-11174100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148834090	chr12:11174105-11174106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369971457	chr12:11174168-11174169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79057393	chr12:11174186-11174187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531805156	chr12:11174203-11174204	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114463974	chr12:11174213-11174214	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79407997	chr12:11174219-11174220	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74363809	chr12:11174223-11174224	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200425184	chr12:11174244-11174245	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77074409	chr12:11174264-11174265	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368242992	chr12:11174274-11174275	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139129245	chr12:11174275-11174276	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10772420	chr12:11174276-11174277	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs74386164	chr12:11174282-11174283	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77837442	chr12:11174286-11174287	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72475480	chr12:11174302-11174303	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554158403	chr12:11174307-11174308	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567559465	chr12:11174319-11174320	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144242846	chr12:11174321-11174322	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72475481	chr12:11174327-11174328	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560133729	chr12:11174356-11174357	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527944519	chr12:11174366-11174367	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74772077	chr12:11174372-11174373	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576069733	chr12:11174373-11174374	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372566412	chr12:11174376-11174377	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76970958	chr12:11174380-11174381	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199776344	chr12:11174382-11174383	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74992161	chr12:11174390-11174391	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76455106	chr12:11174397-11174398	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200784218	chr12:11174402-11174403	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs200427244	chr12:11174408-11174409	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
6	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
9	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
11	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
12	chr12:11148400-11178200	Weak transcription	Dnd41	blood
13	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
14	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:11154200-11178200	Weak transcription	A549	lung
16	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:11159400-11182000	Weak transcription	NHEK	skin
18	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
21	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
23	chr12:11163600-11178800	Weak transcription	Ovary	ovary
24	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
26	chr12:11165000-11180800	Weak transcription	HSMM	muscle
27	chr12:11165400-11180200	Weak transcription	Esophagus	oesophagus
28	chr12:11165600-11174200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr12:11166600-11199600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:11167000-11178200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:11167400-11201800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr12:11167600-11178000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:11167600-11180000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr12:11167800-11178600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr12:11168000-11177600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:11168800-11201000	Weak transcription	Colon Smooth Muscle	Colon
39	chr12:11168800-11205800	Weak transcription	Osteobl	bone
40	chr12:11169000-11177000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:11169000-11178200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:11169000-11180200	Weak transcription	Adipose Nuclei	Adipose
43	chr12:11169200-11174200	Weak transcription	Right Atrium	heart
44	chr12:11169200-11178000	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr12:11169200-11178200	Weak transcription	Liver	Liver
46	chr12:11169400-11174200	Weak transcription	Primary T cells from cord blood	blood
47	chr12:11169400-11176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:11169400-11178000	Weak transcription	Fetal Muscle Leg	muscle
49	chr12:11169400-11180200	Weak transcription	Gastric	stomach
50	chr12:11169400-11180800	Weak transcription	Right Ventricle	heart

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