Variant report

Variant	nsv1044915
Chromosome Location	chr12:9633858-9743799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
2	ARID3A	chr12:9743025-9743373	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:9741257-9741854	HepG2	liver:	n/a	n/a
4	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
5	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
7	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
8	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
10	CEBPB	chr12:9741394-9741705	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
13	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
14	CEBPZ	chr12:9741497-9741533	HepG2	liver:	n/a	n/a
15	CTCF	chr12:9730389-9730511	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:9695807-9695847	GM13976	blood:	n/a	n/a
17	CTCF	chr12:9665444-9665629	K562	blood:	n/a	n/a
18	CTCF	chr12:9665600-9665750	RPTEC	kidney:	n/a	n/a
19	CTCF	chr12:9665360-9665590	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:9665360-9665510	HMF	breast:	n/a	n/a
21	CTCF	chr12:9691647-9691785	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:9723279-9723384	GM19238	blood:	n/a	n/a
23	CTCF	chr12:9665374-9665581	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:9664977-9665006	GM10248	blood:	n/a	n/a
25	CTCF	chr12:9669822-9669862	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr12:9665477-9665516	GM13977	blood:	n/a	n/a
27	CTCF	chr12:9665360-9665558	A549	lung:	n/a	n/a
28	CTCF	chr12:9697887-9697942	GM13977	blood:	n/a	n/a
29	CTCF	chr12:9665424-9665591	GM10266	blood:	n/a	n/a
30	CTCF	chr12:9665352-9665595	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr12:9665359-9665586	Gliobla	brain:	n/a	n/a
32	CTCF	chr12:9665402-9665599	LNCaP	prostate:	n/a	n/a
33	CTCF	chr12:9665294-9665690	A549	lung:	n/a	n/a
34	CTCF	chr12:9726197-9726271	GM20000	blood:	n/a	n/a
35	CTCF	chr12:9634822-9634891	GM12891	blood:	n/a	n/a
36	CTCF	chr12:9634646-9634695	GM12891	blood:	n/a	n/a
37	CTCF	chr12:9665389-9665592	LNCaP	prostate:	n/a	n/a
38	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr12:9665376-9665490	HepG2	liver:	n/a	n/a
40	CTCF	chr12:9730978-9731104	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:9665390-9665555	ProgFib	skin:	n/a	n/a
42	CTCF	chr12:9723300-9723450	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr12:9665369-9665585	GM13976	blood:	n/a	n/a
44	CTCF	chr12:9665411-9665564	GM10248	blood:	n/a	n/a
45	CTCF	chr12:9730398-9730556	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr12:9665315-9665625	A549	lung:	n/a	n/a
47	CTCF	chr12:9665399-9665582	GM12878	blood:	n/a	n/a
48	CTCF	chr12:9719543-9719625	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr12:9634643-9634716	GM19239	blood:	n/a	n/a
50	CTCF	chr12:9665458-9665601	Kidney_OC	kidney:	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	chr12:9720090-9720140	LNCaP	prostate:	n/a
2	chr12:9722091-9722141	ProgFib	skin:	n/a
3	chr12:9723402-9723452	BE2_C	brain:	n/a
4	chr12:9723402-9723452	GM06990	blood:	n/a
5	chr12:9720554-9720604	A549	lung:	n/a
6	chr12:9720554-9720604	SK-N-SH_RA	brain:	n/a
7	chr12:9722091-9722141	ECC-1	luminal epithelium:	n/a
8	chr12:9723402-9723452	PFSK-1	brain:	n/a
9	chr12:9720090-9720140	HAEpiC	amniotic membrane:	n/a
10	chr12:9722091-9722141	HMEC	breast:	n/a
11	chr12:9720090-9720140	NT2-D1	testis:	n/a
12	chr12:9722091-9722141	NB4	blood:	n/a
13	chr12:9720090-9720140	Jurkat	blood:	n/a
14	chr12:9720554-9720604	HRPEpiC	eye:	n/a
15	chr12:9723402-9723452	IMR90	lung:	fetal
16	chr12:9720090-9720140	AG09309	skin:	n/a
17	chr12:9722091-9722141	AG04450	lung:	fetal
18	chr12:9720090-9720140	HRCEpiC	kidney:	n/a
19	chr12:9723402-9723452	SKMC	muscle:	n/a
20	chr12:9720554-9720604	AG09309	skin:	n/a
21	chr12:9723402-9723452	NB4	blood:	n/a
22	chr12:9720090-9720140	HRE	kidney:	n/a
23	chr12:9723402-9723452	RPTEC	kidney:	n/a
24	chr12:9720554-9720604	HMEC	breast:	n/a
25	chr12:9723402-9723452	A549	lung:	n/a
26	chr12:9720090-9720140	T-47D	breast:	n/a
27	chr12:9722091-9722141	HRPEpiC	eye:	n/a
28	chr12:9722091-9722141	AG10803	skin:	n/a
29	chr12:9723402-9723452	ovcar-3	ovarian:	n/a
30	chr12:9720554-9720604	PANC-1	pancreas:	n/a
31	chr12:9720090-9720140	HEEpiC	esophagus:	n/a
32	chr12:9720554-9720604	NHDF-neo	bronchial:	n/a
33	chr12:9720554-9720604	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:9720090-9720140	GM19239	blood:	n/a
35	chr12:9722091-9722141	HUVEC	blood vessel:	n/a
36	chr12:9722091-9722141	T-47D	breast:	n/a
37	chr12:9722091-9722141	HRE	kidney:	n/a
38	chr12:9720554-9720604	Jurkat	blood:	n/a
39	chr12:9723402-9723452	CMK	blood:	n/a
40	chr12:9723402-9723452	ProgFib	skin:	n/a
41	chr12:9722091-9722141	HAEpiC	amniotic membrane:	n/a
42	chr12:9720554-9720604	GM19239	blood:	n/a
43	chr12:9720090-9720140	Hela-S3	cervix:	n/a
44	chr12:9720554-9720604	Hela-S3	cervix:	n/a
45	chr12:9723402-9723452	GM12891	blood:	n/a
46	chr12:9720090-9720140	RPTEC	kidney:	n/a
47	chr12:9720554-9720604	HUVEC	blood vessel:	n/a
48	chr12:9723402-9723452	SAEC	small airway:	n/a
49	chr12:9723402-9723452	HUVEC	blood vessel:	n/a
50	chr12:9722091-9722141	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:
2	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830
2	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
3	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
4	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
5	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
6	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830
7	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830
8	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
9	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island
ENSG00000111796	chromatin interactions

Extended variants
information (count: 2222 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2222 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143709939	chr12:9633873-9633874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78993075	chr12:9633941-9633942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186353838	chr12:9633970-9633971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201315087	chr12:9634004-9634005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552070462	chr12:9634128-9634129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139578221	chr12:9634312-9634313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571891693	chr12:9634314-9634315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2908214	chr12:9634316-9634317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149708883	chr12:9634332-9634333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190754800	chr12:9634409-9634410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369368363	chr12:9634513-9634514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117426113	chr12:9634655-9634656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569644359	chr12:9634702-9634703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76260098	chr12:9634780-9634781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74062860	chr12:9634794-9634795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2536655	chr12:9634837-9634838	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs377639918	chr12:9634855-9634856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144223625	chr12:9634876-9634877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12818352	chr12:9635057-9635058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182912451	chr12:9635106-9635107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371291934	chr12:9635149-9635150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187205116	chr12:9635161-9635162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191557671	chr12:9635163-9635164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141189868	chr12:9635166-9635167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112261963	chr12:9635219-9635220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183422432	chr12:9635228-9635229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187907567	chr12:9635329-9635330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74062861	chr12:9635585-9635586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs116378574	chr12:9635611-9635612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10771797	chr12:9635612-9635613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs113103373	chr12:9635619-9635620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192765282	chr12:9635860-9635861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74062863	chr12:9635970-9635971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs111800806	chr12:9636083-9636084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377430819	chr12:9636087-9636088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183673187	chr12:9636088-9636089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187939278	chr12:9636274-9636275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144496864	chr12:9636380-9636381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375255304	chr12:9636474-9636475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192366655	chr12:9636489-9636490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76279564	chr12:9636566-9636567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142465017	chr12:9636593-9636594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534623525	chr12:9636628-9636629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79193164	chr12:9636776-9636777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77090585	chr12:9636810-9636811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113875535	chr12:9637041-9637042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557581567	chr12:9637105-9637106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76932641	chr12:9637169-9637170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138763154	chr12:9637274-9637275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34039414	chr12:9637402-9637403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:9623200-9653000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:9627000-9663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9638400-9640200	Weak transcription	Fetal Thymus	thymus
5	chr12:9640200-9640600	Enhancers	Fetal Thymus	thymus
6	chr12:9655400-9656000	Enhancers	Dnd41	blood
7	chr12:9657000-9664800	Weak transcription	Fetal Lung	lung
8	chr12:9659400-9662200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:9661800-9663000	Enhancers	Hela-S3	cervix
10	chr12:9662000-9662800	Enhancers	HMEC	breast
11	chr12:9662000-9663400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:9662200-9662600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:9662200-9663000	Enhancers	NHEK	skin
14	chr12:9662200-9663400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:9662400-9662800	Enhancers	HUVEC	blood vessel
16	chr12:9662400-9663000	Enhancers	Osteobl	bone
17	chr12:9662400-9663400	Enhancers	Fetal Heart	heart
18	chr12:9662600-9663000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:9662600-9663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:9662600-9663200	Enhancers	Primary B cells from cord blood	blood
21	chr12:9662600-9664400	Enhancers	Fetal Thymus	thymus
22	chr12:9663000-9663600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr12:9663000-9664200	Enhancers	Thymus	Thymus
24	chr12:9663400-9663600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:9663400-9667200	Weak transcription	Fetal Heart	heart
26	chr12:9663600-9664000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:9664000-9664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:9664200-9702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:9665000-9667800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr12:9667200-9668000	Enhancers	Fetal Heart	heart
31	chr12:9667800-9668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr12:9667800-9668800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr12:9668200-9668800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:9668800-9679600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr12:9679600-9680000	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr12:9686000-9703600	Weak transcription	Hela-S3	cervix
37	chr12:9703600-9705600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:9704000-9721800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:9705600-9706400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:9706400-9735000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:9717000-9717400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr12:9721200-9722400	Weak transcription	Thymus	Thymus
43	chr12:9721400-9723400	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr12:9721800-9722000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:9721800-9722200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr12:9721800-9723000	Active TSS	Right Ventricle	heart
47	chr12:9722000-9723000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:9722000-9723000	ZNF genes & repeats	Fetal Thymus	thymus
49	chr12:9722200-9722400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
50	chr12:9722200-9722800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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