Variant report

Variant	esv12947
Chromosome Location	chr12:751959-752547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:751604-752174	GM12878	blood:	n/a	n/a
2	ATF3	chr12:751751-752142	GM12878	blood:	n/a	chr12:751828-751837
3	ATF3	chr12:751842-752074	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr12:751830-752092	K562	blood:	n/a	n/a
5	BACH1	chr12:751945-752753	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr12:751833-752090	GM12878	blood:	n/a	n/a
7	BCL3	chr12:752331-752877	A549	lung:	n/a	n/a
8	BCL3	chr12:751585-752198	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:751697-753147	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:751703-752097	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:751793-753273	K562	blood:	n/a	chr12:751804-751820
12	BHLHE40	chr12:751566-752695	GM12878	blood:	n/a	chr12:751804-751820
13	CBX3	chr12:752477-753062	K562	blood:	n/a	n/a
14	CCNT2	chr12:751817-752596	K562	blood:	n/a	n/a
15	CEBPB	chr12:752462-752951	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr12:751725-753716	GM12878	blood:	n/a	chr12:751750-751759
17	CHD2	chr12:751766-752686	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr12:751772-752855	GM12878	blood:	n/a	n/a
19	CHD2	chr12:752425-752426	K562	blood:	n/a	n/a
20	CREB1	chr12:751723-752256	A549	lung:	n/a	n/a
21	CTCF	chr12:752260-752410	GM12872	blood:	n/a	n/a
22	CTCF	chr12:752220-752370	AG09309	skin:	n/a	n/a
23	CTCF	chr12:752280-752430	GM12873	blood:	n/a	n/a
24	CTCF	chr12:752380-752530	AG04450	lung:	n/a	n/a
25	CTCF	chr12:752271-752470	K562	blood:	n/a	n/a
26	CTCF	chr12:752520-752670	NHLF	lung:	n/a	n/a
27	CTCF	chr12:752260-752410	GM12865	blood:	n/a	n/a
28	CTCF	chr12:752237-752552	GM19239	blood:	n/a	n/a
29	CTCF	chr12:752220-752370	BJ	skin:	n/a	n/a
30	CTCF	chr12:752542-752627	GM19240	blood:	n/a	n/a
31	CTCF	chr12:752280-752430	GM12865	blood:	n/a	n/a
32	CTCF	chr12:752259-752400	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr12:752280-752430	NHLF	lung:	n/a	n/a
34	CTCF	chr12:752260-752410	HPF	lung:	n/a	n/a
35	CTCF	chr12:752254-752481	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:752260-752410	GM12869	blood:	n/a	n/a
37	CTCF	chr12:752160-752310	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr12:752260-752410	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr12:752240-752474	GM12891	blood:	n/a	n/a
40	CTCF	chr12:752260-752410	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr12:752220-752370	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr12:752220-752370	HCT-116	colon:	n/a	n/a
43	CTCF	chr12:752280-752430	Caco-2	colon:	n/a	n/a
44	CTCF	chr12:752260-752410	BJ	skin:	n/a	n/a
45	CTCF	chr12:752300-752450	Caco-2	colon:	n/a	n/a
46	CTCF	chr12:752188-753187	K562	blood:	n/a	n/a
47	CTCF	chr12:752253-752504	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:752177-752558	K562	blood:	n/a	n/a
49	CTCF	chr12:752260-752410	K562	blood:	n/a	n/a
50	CTCF	chr12:752280-752430	GM12870	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:752381-752431	HCT-116	colon:	n/a
2	chr12:752381-752431	GM12892	blood:	n/a
3	chr12:752290-752340	ECC-1	luminal epithelium:	n/a
4	chr12:752290-752340	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:752381-752431	SAEC	small airway:	n/a
6	chr12:752381-752431	ProgFib	skin:	n/a
7	chr12:752381-752431	HL-60	blood:	n/a
8	chr12:752381-752431	PrEC	prostate:	n/a
9	chr12:752290-752340	NHBE	bronchial:	n/a
10	chr12:752381-752431	AG09309	skin:	n/a
11	chr12:752381-752431	AG04449	skin:	fetal
12	chr12:752381-752431	ECC-1	luminal epithelium:	n/a
13	chr12:752290-752340	IMR90	lung:	fetal
14	chr12:752381-752431	NHDF-neo	bronchial:	n/a
15	chr12:752381-752431	MCF-7	breast:	n/a
16	chr12:752290-752340	LNCaP	prostate:	n/a
17	chr12:752381-752431	SK-N-SH	brain:	n/a
18	chr12:752290-752340	ProgFib	skin:	n/a
19	chr12:752290-752340	T-47D	breast:	n/a
20	chr12:752290-752340	AoSMC	blood vessel:	n/a
21	chr12:752381-752431	AG09319	gingival:	n/a
22	chr12:752290-752340	PFSK-1	brain:	n/a
23	chr12:752381-752431	GM19239	blood:	n/a
24	chr12:752290-752340	SAEC	small airway:	n/a
25	chr12:752290-752340	HMEC	breast:	n/a
26	chr12:752381-752431	HIPEpiC	eye:	n/a
27	chr12:752290-752340	Hela-S3	cervix:	n/a
28	chr12:752381-752431	PANC-1	pancreas:	n/a
29	chr12:752381-752431	LNCaP	prostate:	n/a
30	chr12:752381-752431	HEEpiC	esophagus:	n/a
31	chr12:752381-752431	RPTEC	kidney:	n/a
32	chr12:752381-752431	T-47D	breast:	n/a
33	chr12:752381-752431	SK-N-MC	brain:	n/a
34	chr12:752290-752340	RPTEC	kidney:	n/a
35	chr12:752290-752340	ovcar-3	ovarian:	n/a
36	chr12:752290-752340	HUVEC	blood vessel:	n/a
37	chr12:752290-752340	PANC-1	pancreas:	n/a
38	chr12:752381-752431	SK-N-SH_RA	brain:	n/a
39	chr12:752381-752431	HRE	kidney:	n/a
40	chr12:752290-752340	MCF-7	breast:	n/a
41	chr12:752381-752431	PFSK-1	brain:	n/a
42	chr12:752290-752340	A549	lung:	n/a
43	chr12:752290-752340	Jurkat	blood:	n/a
44	chr12:752381-752431	A549	lung:	n/a
45	chr12:752290-752340	HRPEpiC	eye:	n/a
46	chr12:752290-752340	HEK293	kidney:	embryo
47	chr12:752290-752340	GM12878	blood:	n/a
48	chr12:752290-752340	HL-60	blood:	n/a
49	chr12:752381-752431	AG04450	lung:	fetal
50	chr12:752290-752340	AG10803	skin:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:749727..757562-chr12:858273..868886,17	MCF-7	breast:
2	chr12:749128..755954-chr12:858463..864495,7	MCF-7	breast:
3	chr12:751801..754339-chr12:772154..775493,3	MCF-7	breast:
4	chr12:752081..752621-chr15:68569750..68570655,2	HCT-116	colon:
5	chr12:751953..754697-chr12:859970..862221,2	K562	blood:
6	chr12:750256..753677-chr12:768929..774136,4	MCF-7	breast:
7	chr12:751220..755551-chr12:860416..865761,8	K562	blood:
8	chr12:508524..511172-chr12:751040..752702,2	MCF-7	breast:
9	chr12:739608..744885-chr12:750259..753818,8	MCF-7	breast:
10	chr12:738549..743434-chr12:750658..753859,6	MCF-7	breast:
11	chr12:698993..700663-chr12:750297..752796,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALNT3-2	chr12:752514-753003	NONHSAT025360
2	lnc-B4GALNT3-2	chr12:752147-752883	ENSG00000177406.4

No data

Variant related genes	Relation type
ENSG00000177406	TF binding region
ENSG00000177406	CpG island
ENSG00000255825	chromatin interactions
ENSG00000260657	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000060237	chromatin interactions
ENSG00000177406	chromatin interactions
ENSG00000171840	chromatin interactions
ENSG00000169018	chromatin interactions

Extended variants
information (count: 26 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111932820	chr12:751964-751965	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs552681084	chr12:751981-751982	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs570514422	chr12:751984-751985	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs544074093	chr12:752086-752087	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs541269975	chr12:752092-752093	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs534820476	chr12:752127-752128	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs527733162	chr12:752181-752182	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
8	rs368283046	chr12:752202-752203	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
9	rs568031297	chr12:752205-752206	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
10	rs535396970	chr12:752209-752210	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
11	rs556519954	chr12:752218-752219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
12	rs575232800	chr12:752252-752253	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
13	rs558243295	chr12:752273-752274	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
14	rs575408963	chr12:752319-752320	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
15	rs6489690	chr12:752327-752328	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs55800929	chr12:752360-752361	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs115303052	chr12:752395-752396	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
18	rs560022147	chr12:752415-752416	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs149445485	chr12:752420-752421	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs528752721	chr12:752438-752439	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs542591870	chr12:752450-752451	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs563524916	chr12:752459-752460	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs530538390	chr12:752472-752473	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
24	rs368511391	chr12:752477-752478	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
25	rs371838855	chr12:752520-752521	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
26	rs552343109	chr12:752533-752534	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:742400-752200	Weak transcription	Brain Substantia Nigra	brain
2	chr12:747400-752200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:747400-754000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:749400-752200	Weak transcription	HUVEC	blood vessel
5	chr12:749400-752400	Weak transcription	HSMMtube	muscle
6	chr12:750200-753200	Weak transcription	HepG2	liver
7	chr12:750400-752200	Weak transcription	NHEK	skin
8	chr12:750800-752200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr12:751200-752000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr12:751200-752200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr12:751200-752400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:751200-752400	Active TSS	Brain Hippocampus Middle	brain
13	chr12:751200-752400	Active TSS	Stomach Smooth Muscle	stomach
14	chr12:751200-752600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr12:751200-752600	Active TSS	Brain Anterior Caudate	brain
16	chr12:751200-752800	Active TSS	Brain Germinal Matrix	brain
17	chr12:751400-752000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
18	chr12:751400-752200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:751400-752200	Weak transcription	Spleen	Spleen
20	chr12:751400-752200	Weak transcription	K562	blood
21	chr12:751400-752400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr12:751400-752400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr12:751400-752400	Active TSS	Brain Cingulate Gyrus	brain
24	chr12:751400-752400	Active TSS	Fetal Muscle Leg	muscle
25	chr12:751400-752600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:751400-752600	Active TSS	Duodenum Mucosa	Duodenum
27	chr12:751400-752600	Active TSS	Fetal Intestine Small	intestine
28	chr12:751400-752600	Active TSS	Fetal Lung	lung
29	chr12:751400-752600	Active TSS	Fetal Stomach	stomach
30	chr12:751400-752600	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr12:751400-752800	Active TSS	Brain Angular Gyrus	brain
32	chr12:751400-753200	Active TSS	H9 Cell Line	embryonic stem cell
33	chr12:751600-752000	Flanking Active TSS	Primary B cells from peripheral blood	blood
34	chr12:751600-752000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:751600-752000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:751600-752200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr12:751600-752200	Weak transcription	Primary T cells from cord blood	blood
38	chr12:751600-752200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr12:751600-752200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:751600-752200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr12:751600-752200	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr12:751600-752400	Active TSS	H1 Cell Line	embryonic stem cell
43	chr12:751600-752400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:751600-752400	Active TSS	Adipose Nuclei	Adipose
45	chr12:751600-752400	Active TSS	Colonic Mucosa	Colon
46	chr12:751600-752400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr12:751600-752400	Active TSS	Placenta Amnion	Placenta Amnion
48	chr12:751600-752400	Active TSS	Rectal Smooth Muscle	rectum
49	chr12:751600-752400	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr12:751600-752400	Active TSS	A549	lung

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