Variant report

Variant	nsv556993
Chromosome Location	chr12:1703070-1704325
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	ATF3	chr12:1703979-1704186	K562	blood:	n/a	n/a
2	ATF3	chr12:1703905-1704290	A549	lung:	n/a	n/a
3	ATF3	chr12:1703691-1704192	A549	lung:	n/a	n/a
4	ATF3	chr12:1703921-1704219	HepG2	liver:	n/a	n/a
5	BACH1	chr12:1704012-1704359	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr12:1702399-1703218	A549	lung:	n/a	n/a
7	BCL3	chr12:1702811-1703565	GM12878	blood:	n/a	chr12:1703277-1703290 chr12:1703246-1703255 chr12:1703251-1703264
8	BCLAF1	chr12:1703326-1703559	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:1703961-1704290	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:1702596-1703225	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:1702937-1703126	K562	blood:	n/a	n/a
12	BHLHE40	chr12:1703615-1704317	K562	blood:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
13	BHLHE40	chr12:1703132-1704326	GM12878	blood:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703282-1703298 chr12:1703887-1703903
14	BHLHE40	chr12:1703541-1704274	HepG2	liver:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
15	BHLHE40	chr12:1703673-1704161	A549	lung:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
16	BRCA1	chr12:1703950-1704220	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr12:1704098-1704155	HepG2	liver:	n/a	n/a
18	BRCA1	chr12:1704097-1704217	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr12:1704032-1704330	K562	blood:	n/a	n/a
20	CCNT2	chr12:1701679-1704259	K562	blood:	n/a	chr12:1701691-1701700 chr12:1704222-1704231
21	CEBPB	chr12:1703958-1704201	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr12:1703267-1703620	HepG2	liver:	n/a	n/a
23	CHD1	chr12:1703705-1704169	H1-hESC	embryonic stem cell:	n/a	chr12:1703926-1703936
24	CHD1	chr12:1701397-1706266	IMR90	lung:	n/a	chr12:1703237-1703247 chr12:1704434-1704444 chr12:1703259-1703269 chr12:1703926-1703936
25	CHD1	chr12:1702663-1704334	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269 chr12:1703926-1703936
26	CHD1	chr12:1702989-1703140	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr12:1701565-1703513	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269
28	CHD2	chr12:1702835-1704367	Hela-S3	cervix:	n/a	chr12:1703237-1703247 chr12:1703259-1703269 chr12:1703926-1703936
29	CHD2	chr12:1703767-1704188	K562	blood:	n/a	chr12:1703926-1703936
30	CHD2	chr12:1702989-1703142	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr12:1703861-1704103	HepG2	liver:	n/a	chr12:1703926-1703936
32	CREB1	chr12:1703583-1704242	A549	lung:	n/a	n/a
33	CREB1	chr12:1702782-1703562	A549	lung:	n/a	n/a
34	CTBP2	chr12:1703753-1704215	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr12:1701629-1703245	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr12:1703048-1703173	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:1704080-1704230	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr12:1703141-1703144	GM12891	blood:	n/a	n/a
39	CTCF	chr12:1704134-1704149	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:1704160-1704310	HCM	heart:	n/a	n/a
41	CTCF	chr12:1703560-1703710	GM12871	blood:	n/a	n/a
42	CTCF	chr12:1704094-1704207	A549	lung:	n/a	n/a
43	CTCF	chr12:1703120-1703134	GM12891	blood:	n/a	n/a
44	CTCF	chr12:1703920-1704070	GM12873	blood:	n/a	n/a
45	CTCF	chr12:1704071-1704239	GM12891	blood:	n/a	n/a
46	CTCF	chr12:1702980-1703130	Caco-2	colon:	n/a	n/a
47	CTCF	chr12:1704080-1704230	K562	blood:	n/a	n/a
48	CTCF	chr12:1704097-1704185	GM10266	blood:	n/a	n/a
49	CTCF	chr12:1703060-1703210	GM12871	blood:	n/a	n/a
50	CTCF	chr12:1703949-1704267	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1704263-1704313	SK-N-SH	brain:	n/a
2	chr12:1703169-1703219	SK-N-SH_RA	brain:	n/a
3	chr12:1703169-1703219	AG09309	skin:	n/a
4	chr12:1704065-1704115	GM12892	blood:	n/a
5	chr12:1704156-1704206	T-47D	breast:	n/a
6	chr12:1703181-1703231	HIPEpiC	eye:	n/a
7	chr12:1704263-1704313	PANC-1	pancreas:	n/a
8	chr12:1704263-1704313	CMK	blood:	n/a
9	chr12:1704080-1704130	HNPCEpiC	eye:	n/a
10	chr12:1703181-1703231	K562	blood:	n/a
11	chr12:1703169-1703219	HRCEpiC	kidney:	n/a
12	chr12:1703704-1703754	ECC-1	luminal epithelium:	n/a
13	chr12:1703169-1703219	HCT-116	colon:	n/a
14	chr12:1703181-1703231	GM12892	blood:	n/a
15	chr12:1703181-1703231	GM19239	blood:	n/a
16	chr12:1703704-1703754	ovcar-3	ovarian:	n/a
17	chr12:1704263-1704313	HIPEpiC	eye:	n/a
18	chr12:1704080-1704130	PFSK-1	brain:	n/a
19	chr12:1704263-1704313	T-47D	breast:	n/a
20	chr12:1704156-1704206	SKMC	muscle:	n/a
21	chr12:1704080-1704130	MCF10A-Er-Src	breast:	n/a
22	chr12:1704065-1704115	IMR90	lung:	fetal
23	chr12:1703181-1703231	SAEC	small airway:	n/a
24	chr12:1704263-1704313	HCT-116	colon:	n/a
25	chr12:1703181-1703231	CMK	blood:	n/a
26	chr12:1703181-1703231	GM06990	blood:	n/a
27	chr12:1703704-1703754	U87	brain:	n/a
28	chr12:1704156-1704206	HepG2	liver:	n/a
29	chr12:1704156-1704206	GM06990	blood:	n/a
30	chr12:1704263-1704313	MCF10A-Er-Src	breast:	n/a
31	chr12:1703704-1703754	IMR90	lung:	fetal
32	chr12:1704065-1704115	HCPEpiC	choroid plexus:	n/a
33	chr12:1704080-1704130	AG04449	skin:	fetal
34	chr12:1704080-1704130	HMEC	breast:	n/a
35	chr12:1704065-1704115	NB4	blood:	n/a
36	chr12:1704263-1704313	ProgFib	skin:	n/a
37	chr12:1703181-1703231	HCPEpiC	choroid plexus:	n/a
38	chr12:1703169-1703219	AG04449	skin:	fetal
39	chr12:1703704-1703754	HRPEpiC	eye:	n/a
40	chr12:1704156-1704206	LNCaP	prostate:	n/a
41	chr12:1704065-1704115	RPTEC	kidney:	n/a
42	chr12:1704080-1704130	HRCEpiC	kidney:	n/a
43	chr12:1704065-1704115	AG10803	skin:	n/a
44	chr12:1704065-1704115	HMEC	breast:	n/a
45	chr12:1704156-1704206	HCM	heart:	n/a
46	chr12:1703169-1703219	A549	lung:	n/a
47	chr12:1704263-1704313	HCF	heart:	n/a
48	chr12:1704065-1704115	HCM	heart:	n/a
49	chr12:1704080-1704130	H1-hESC	embryonic stem cell:	embryo
50	chr12:1704156-1704206	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1224466..1226137-chr12:1702484..1704918,2	MCF-7	breast:
2	chr11:64645557..64646112-chr12:1703529..1704108,2	Hela-S3	cervix:
3	chr12:1700363..1702369-chr12:1703399..1707703,4	K562	blood:
4	chr12:1703157..1705505-chr12:1739226..1741204,2	MCF-7	breast:
5	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:
6	chr12:1703565..1707939-chr12:1709383..1712701,6	MCF-7	breast:
7	chr12:547432..549780-chr12:1702241..1704941,2	MCF-7	breast:
8	chr12:1703685..1705372-chr12:1898619..1900530,2	K562	blood:
9	chr12:1703426..1704364-chr18:71959175..71959778,2	NB4	blood:
10	chr12:1703509..1704108-chr6:26216519..26217376,2	Hela-S3	cervix:

Variant related genes	Relation type
FBXL14	TF binding region
FBXL14	CpG island
ENSG00000168274	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000082805	chromatin interactions
ENSG00000111186	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000171823	chromatin interactions
ENSG00000166347	chromatin interactions
ENSG00000110047	chromatin interactions

Extended variants
information (count: 33 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376933643	chr12:1703077-1703078	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs368750848	chr12:1703095-1703096	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs373403328	chr12:1703097-1703098	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs376652993	chr12:1703167-1703168	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs577325408	chr12:1703185-1703186	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs201556394	chr12:1703226-1703227	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs111814721	chr12:1703246-1703247	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs541686360	chr12:1703264-1703265	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs548123930	chr12:1703281-1703282	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs559883431	chr12:1703312-1703313	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs563440973	chr12:1703322-1703323	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs544992054	chr12:1703323-1703324	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs575015772	chr12:1703365-1703366	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs549524374	chr12:1703415-1703416	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs542229686	chr12:1703642-1703643	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs563501829	chr12:1703740-1703741	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs530958233	chr12:1703803-1703804	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs552142815	chr12:1703819-1703820	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs564418172	chr12:1703854-1703855	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs369427877	chr12:1703976-1703977	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs557829617	chr12:1703978-1703979	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs11061871	chr12:1703987-1703988	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs546414735	chr12:1703989-1703990	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs147317714	chr12:1704121-1704122	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs547385949	chr12:1704130-1704131	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs535142537	chr12:1704151-1704152	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs201519750	chr12:1704160-1704161	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs67277632	chr12:1704165-1704166	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs35749496	chr12:1704168-1704169	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs113961848	chr12:1704182-1704183	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs75067473	chr12:1704183-1704184	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs558977671	chr12:1704218-1704219	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs577658537	chr12:1704286-1704287	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1699200-1703200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:1699600-1703200	Flanking Active TSS	HMEC	breast
3	chr12:1699800-1703200	Flanking Active TSS	HUVEC	blood vessel
4	chr12:1700000-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:1700400-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:1700400-1703200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr12:1700600-1703200	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr12:1700600-1704400	Active TSS	Brain Germinal Matrix	brain
9	chr12:1700800-1704600	Active TSS	Ovary	ovary
10	chr12:1701000-1704800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr12:1701200-1703200	Active TSS	Stomach Mucosa	stomach
12	chr12:1701200-1704200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr12:1701400-1703200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:1701400-1703200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr12:1701600-1703200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr12:1701600-1703200	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr12:1701600-1703200	Flanking Active TSS	Colonic Mucosa	Colon
18	chr12:1701600-1703200	Flanking Active TSS	Placenta	Placenta
19	chr12:1701600-1703200	Flanking Active TSS	NH-A	brain
20	chr12:1701800-1703200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
21	chr12:1701800-1703200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr12:1701800-1704400	Active TSS	Fetal Kidney	kidney
23	chr12:1701800-1704600	Active TSS	Small Intestine	intestine
24	chr12:1702400-1703200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr12:1702400-1703200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:1702400-1703200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr12:1702400-1703200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
28	chr12:1702400-1703200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
29	chr12:1702400-1703200	Active TSS	NHDF-Ad	bronchial
30	chr12:1702400-1704200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:1702400-1704400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr12:1702400-1705000	Active TSS	Right Atrium	heart
33	chr12:1702600-1703200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:1702600-1703200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:1702600-1703200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr12:1702600-1703200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:1702600-1703200	Flanking Active TSS	Fetal Muscle Trunk	muscle
38	chr12:1702600-1704200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:1702600-1704200	Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr12:1702600-1704200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr12:1702600-1704200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:1702600-1704200	Active TSS	Rectal Smooth Muscle	rectum
43	chr12:1702600-1704400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:1702600-1704400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr12:1702600-1704400	Active TSS	Primary T cells from cord blood	blood
46	chr12:1702600-1704400	Active TSS	Brain Angular Gyrus	brain
47	chr12:1702600-1704400	Active TSS	Brain Anterior Caudate	brain
48	chr12:1702600-1704400	Active TSS	Colon Smooth Muscle	Colon
49	chr12:1702600-1704400	Active TSS	Lung	lung
50	chr12:1702600-1704400	Active TSS	Thymus	Thymus

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