Variant report

Variant	esv2558829
Chromosome Location	chr12:62992678-62994139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:62993920-62994070	BE2_C	brain:	n/a	chr12:62993981-62993988
2	CTCF	chr12:62993900-62994050	GM12864	blood:	n/a	chr12:62993981-62993988
3	CTCF	chr12:62994080-62994230	HCM	heart:	n/a	n/a
4	CTCF	chr12:62993920-62994070	GM12878	blood:	n/a	chr12:62993981-62993988
5	CTCF	chr12:62993960-62994110	NHEK	skin:	n/a	chr12:62993981-62993988
6	CTCF	chr12:62993940-62994090	HFF-Myc	foreskin:	n/a	chr12:62993981-62993988
7	CTCF	chr12:62993900-62994050	NHLF	lung:	n/a	chr12:62993981-62993988
8	CTCF	chr12:62993900-62994050	HUVEC	blood vessel:	n/a	chr12:62993981-62993988
9	CTCF	chr12:62993920-62994070	HPAF	blood vessel:	n/a	chr12:62993981-62993988
10	CTCF	chr12:62993900-62994050	HEK293	kidney:	n/a	chr12:62993981-62993988
11	CTCF	chr12:62993960-62994110	GM06990	blood:	n/a	chr12:62993981-62993988
12	CTCF	chr12:62993900-62994050	NHDF-neo	bronchial:	n/a	chr12:62993981-62993988
13	CTCF	chr12:62993937-62994009	GM13977	blood:	n/a	chr12:62993981-62993988
14	CTCF	chr12:62993860-62994010	NB4	blood:	n/a	chr12:62993981-62993988
15	CTCF	chr12:62993940-62994090	HEEpiC	esophagus:	n/a	chr12:62993981-62993988
16	CTCF	chr12:62993820-62993970	GM12868	blood:	n/a	n/a
17	CTCF	chr12:62993940-62994090	AG09319	gingival:	n/a	chr12:62993981-62993988
18	CTCF	chr12:62993840-62993990	GM12874	blood:	n/a	chr12:62993981-62993988
19	CTCF	chr12:62993860-62994010	AoAF	blood vessel:	n/a	chr12:62993981-62993988
20	CTCF	chr12:62993940-62994090	RPTEC	kidney:	n/a	chr12:62993981-62993988
21	CTCF	chr12:62993820-62993970	GM12872	blood:	n/a	n/a
22	CTCF	chr12:62993812-62994137	K562	blood:	n/a	chr12:62993981-62993988
23	CTCF	chr12:62993860-62994010	HMEC	breast:	n/a	chr12:62993981-62993988
24	CTCF	chr12:62993880-62994030	SAEC	small airway:	n/a	chr12:62993981-62993988
25	CTCF	chr12:62993900-62994050	SK-N-SH_RA	brain:	n/a	chr12:62993981-62993988
26	CTCF	chr12:62993900-62994050	AoAF	blood vessel:	n/a	chr12:62993981-62993988
27	CTCF	chr12:62993920-62994070	Hela-S3	cervix:	n/a	chr12:62993981-62993988
28	CTCF	chr12:62993880-62994030	HA-sp	spinal cord:	n/a	chr12:62993981-62993988
29	CTCF	chr12:62993920-62994070	A549	lung:	n/a	chr12:62993981-62993988
30	CTCF	chr12:62993880-62994030	GM12870	blood:	n/a	chr12:62993981-62993988
31	CTCF	chr12:62993960-62994110	HVMF	connective:	n/a	chr12:62993981-62993988
32	CTCF	chr12:62993860-62994010	HPF	lung:	n/a	chr12:62993981-62993988
33	CTCF	chr12:62993860-62994010	Caco-2	colon:	n/a	chr12:62993981-62993988
34	CTCF	chr12:62993920-62994070	GM12866	blood:	n/a	chr12:62993981-62993988
35	CTCF	chr12:62993955-62994005	K562	blood:	n/a	chr12:62993981-62993988
36	CTCF	chr12:62993880-62994030	HepG2	liver:	n/a	chr12:62993981-62993988
37	CTCF	chr12:62993340-62993490	AG04450	lung:	n/a	n/a
38	CTCF	chr12:62993920-62994070	HAc	cerebellar:	n/a	chr12:62993981-62993988
39	CTCF	chr12:62993880-62994030	AG10803	skin:	n/a	chr12:62993981-62993988
40	CTCF	chr12:62993760-62993910	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr12:62993920-62994070	HFF	foreskin:	n/a	chr12:62993981-62993988
42	CTCF	chr12:62993900-62994050	HBMEC	blood vessel:	n/a	chr12:62993981-62993988
43	CTCF	chr12:62993940-62994090	HCT-116	colon:	n/a	chr12:62993981-62993988
44	CTCF	chr12:62993880-62994030	RPTEC	kidney:	n/a	chr12:62993981-62993988
45	CTCF	chr12:62993860-62994010	GM12875	blood:	n/a	chr12:62993981-62993988
46	CTCF	chr12:62993920-62994070	MCF-7	breast:	n/a	chr12:62993981-62993988
47	CTCF	chr12:62993900-62994050	HA-sp	spinal cord:	n/a	chr12:62993981-62993988
48	CTCF	chr12:62993944-62994054	GM12878	blood:	n/a	chr12:62993981-62993988
49	CTCF	chr12:62993920-62994070	HEEpiC	esophagus:	n/a	chr12:62993981-62993988
50	CTCF	chr12:62993812-62994161	IMR90	lung:	n/a	chr12:62993981-62993988

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62992859-62992909	ovcar-3	ovarian:	n/a
2	chr12:62992859-62992909	T-47D	breast:	n/a
3	chr12:62992859-62992909	GM12891	blood:	n/a
4	chr12:62992859-62992909	NH-A	brain:	n/a
5	chr12:62992859-62992909	BE2_C	brain:	n/a
6	chr12:62992859-62992909	BJ	skin:	n/a
7	chr12:62992859-62992909	NT2-D1	testis:	n/a
8	chr12:62992859-62992909	HEK293	kidney:	embryo
9	chr12:62992859-62992909	K562	blood:	n/a
10	chr12:62992859-62992909	AG04450	lung:	fetal
11	chr12:62992859-62992909	HCT-116	colon:	n/a
12	chr12:62992859-62992909	MCF-7	breast:	n/a
13	chr12:62992859-62992909	NB4	blood:	n/a
14	chr12:62992859-62992909	AG10803	skin:	n/a
15	chr12:62992859-62992909	SKMC	muscle:	n/a
16	chr12:62992859-62992909	A549	lung:	n/a
17	chr12:62992859-62992909	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:62992859-62992909	U87	brain:	n/a
19	chr12:62992859-62992909	HCF	heart:	n/a
20	chr12:62992859-62992909	ProgFib	skin:	n/a
21	chr12:62992859-62992909	GM12892	blood:	n/a
22	chr12:62992859-62992909	GM06990	blood:	n/a
23	chr12:62992859-62992909	AG09309	skin:	n/a
24	chr12:62992859-62992909	ECC-1	luminal epithelium:	n/a
25	chr12:62992859-62992909	RPTEC	kidney:	n/a
26	chr12:62992859-62992909	Jurkat	blood:	n/a
27	chr12:62992859-62992909	SK-N-MC	brain:	n/a
28	chr12:62992859-62992909	HEEpiC	esophagus:	n/a
29	chr12:62992859-62992909	HRPEpiC	eye:	n/a
30	chr12:62992859-62992909	HL-60	blood:	n/a
31	chr12:62992859-62992909	HUVEC	blood vessel:	n/a
32	chr12:62992859-62992909	AG09319	gingival:	n/a
33	chr12:62992859-62992909	H1-hESC	embryonic stem cell:	embryo
34	chr12:62992859-62992909	HepG2	liver:	n/a
35	chr12:62992859-62992909	HIPEpiC	eye:	n/a
36	chr12:62992859-62992909	HCM	heart:	n/a
37	chr12:62992859-62992909	PANC-1	pancreas:	n/a
38	chr12:62992859-62992909	GM12878	blood:	n/a
39	chr12:62992859-62992909	Hepatocyte	liver:	n/a
40	chr12:62992859-62992909	AoSMC	blood vessel:	n/a
41	chr12:62992859-62992909	Caco-2	colon:	n/a
42	chr12:62992859-62992909	MCF10A-Er-Src	breast:	n/a
43	chr12:62992859-62992909	SK-N-SH	brain:	n/a
44	chr12:62992859-62992909	HRCEpiC	kidney:	n/a
45	chr12:62992859-62992909	PFSK-1	brain:	n/a
46	chr12:62992859-62992909	LNCaP	prostate:	n/a
47	chr12:62992859-62992909	HCPEpiC	choroid plexus:	n/a
48	chr12:62992859-62992909	NHBE	bronchial:	n/a
49	chr12:62992859-62992909	Hela-S3	cervix:	n/a
50	chr12:62992859-62992909	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:62916495..62918610-chr12:62994074..62996393,2	MCF-7	breast:
2	chr1:155099354..155102099-chr12:62992358..62995047,2	MCF-7	breast:
3	chr12:62989825..62992021-chr12:62992678..62994199,2	MCF-7	breast:
4	chr12:62979289..62980893-chr12:62991246..62992816,2	K562	blood:
5	chr12:62993913..62996501-chr9:136325777..136327480,2	MCF-7	breast:
6	chr12:62992552..62995339-chr12:63185731..63187957,2	MCF-7	breast:
7	chr12:62991974..62994921-chr5:128794290..128796953,2	MCF-7	breast:
8	chr12:62993534..62994890-chr12:63187464..63188240,4	MCF-7	breast:
9	chr12:62990224..62992773-chr12:63153301..63155013,2	K562	blood:
10	chr12:62978537..62982109-chr12:62993246..62999032,10	MCF-7	breast:
11	chr12:62975484..62979404-chr12:62993353..62996237,5	K562	blood:
12	chr12:62983638..62988242-chr12:62993831..62996165,4	K562	blood:
13	chr12:62974220..62976300-chr12:62991130..62993650,2	MCF-7	breast:

Variant related genes	Relation type
MIRLET7I	TF binding region
ENSG00000257354	TF binding region
MIRLET7I	CpG island
ENSG00000257354	CpG island
ENSG00000249421	chromatin interactions
ENSG00000145808	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000061987	chromatin interactions
ENSG00000169242	chromatin interactions

Extended variants
information (count: 39 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563526329	chr12:62992697-62992698	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs532369834	chr12:62992712-62992713	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs560040622	chr12:62992764-62992765	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs552436453	chr12:62992839-62992840	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs187153830	chr12:62992857-62992858	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs145938756	chr12:62992859-62992860	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs566641181	chr12:62992862-62992863	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs200855569	chr12:62992894-62992895	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs34135257	chr12:62992897-62992898	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs398019871	chr12:62992906-62992907	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs548259175	chr12:62992931-62992932	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs567974149	chr12:62993000-62993001	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs139787635	chr12:62993024-62993025	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs557394522	chr12:62993070-62993071	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs570778737	chr12:62993111-62993112	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs143174242	chr12:62993150-62993151	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs35249679	chr12:62993154-62993155	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs369338402	chr12:62993155-62993156	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs191099677	chr12:62993214-62993215	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs573096995	chr12:62993235-62993236	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537454613	chr12:62993245-62993246	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs541997599	chr12:62993266-62993267	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs146684733	chr12:62993273-62993274	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs377620921	chr12:62993286-62993287	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs575551600	chr12:62993289-62993290	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs545246066	chr12:62993290-62993291	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs529083381	chr12:62993314-62993315	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs557418908	chr12:62993356-62993357	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs12580048	chr12:62993793-62993794	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532476447	chr12:62993798-62993799	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs546117301	chr12:62993800-62993801	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs549225817	chr12:62993831-62993832	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs540405010	chr12:62993839-62993840	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs76484155	chr12:62993921-62993922	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs7311194	chr12:62993936-62993937	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11174558	chr12:62993942-62993943	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182658877	chr12:62993952-62993953	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs140299000	chr12:62994123-62994124	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs186550631	chr12:62994126-62994127	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62917200-62995000	Weak transcription	Fetal Heart	heart
2	chr12:62928800-62995800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:62938000-62995400	Weak transcription	Stomach Mucosa	stomach
4	chr12:62950400-62995600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:62950600-62996200	Weak transcription	Small Intestine	intestine
6	chr12:62950800-62995000	Weak transcription	NHEK	skin
7	chr12:62951000-62995600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:62951200-62995200	Weak transcription	Hela-S3	cervix
9	chr12:62951200-62995600	Weak transcription	HSMMtube	muscle
10	chr12:62951400-62995000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr12:62953400-62996000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:62954800-62995600	Weak transcription	Brain Anterior Caudate	brain
13	chr12:62955200-62995200	Weak transcription	HepG2	liver
14	chr12:62955600-62995600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:62957000-62995600	Weak transcription	Fetal Brain Male	brain
16	chr12:62957200-62995600	Weak transcription	Brain Hippocampus Middle	brain
17	chr12:62959600-62995600	Weak transcription	NHLF	lung
18	chr12:62961200-62995600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr12:62961400-62995600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr12:62961400-62995600	Weak transcription	Brain Germinal Matrix	brain
21	chr12:62961600-62995600	Weak transcription	Fetal Brain Female	brain
22	chr12:62961800-62995600	Weak transcription	Brain Substantia Nigra	brain
23	chr12:62962000-62995600	Weak transcription	HMEC	breast
24	chr12:62963200-62995600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:62964000-62995800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr12:62965400-62992800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr12:62966200-62995600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr12:62966200-62995600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr12:62966400-62995600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr12:62966400-62995600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr12:62966600-62995600	Weak transcription	Thymus	Thymus
32	chr12:62966600-62996000	Weak transcription	Esophagus	oesophagus
33	chr12:62969000-62995600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr12:62969000-62996000	Weak transcription	Left Ventricle	heart
35	chr12:62969000-62996000	Weak transcription	Ovary	ovary
36	chr12:62970000-62995200	Weak transcription	Fetal Lung	lung
37	chr12:62977200-62993400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr12:62978200-62995600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr12:62979200-62995600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr12:62980000-62993400	Weak transcription	GM12878-XiMat	blood
41	chr12:62980000-62993600	Weak transcription	K562	blood
42	chr12:62980000-62995600	Weak transcription	Primary T cells from cord blood	blood
43	chr12:62980000-62995600	Weak transcription	Duodenum Mucosa	Duodenum
44	chr12:62981000-62995200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:62981000-62995400	Weak transcription	Dnd41	blood
46	chr12:62981000-62995600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:62981600-62996000	Weak transcription	Aorta	Aorta
48	chr12:62982000-62995600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:62983000-62993000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr12:62983000-62993200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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