Variant report

Variant	nsv560439
Chromosome Location	chr12:121340246-121341529
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	BACH1	chr12:121341177-121341437	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr12:121340420-121340494	K562	blood:	n/a	n/a
3	BHLHE40	chr12:121341176-121341570	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:121341270-121341314	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr12:121341420-121341445	HepG2	liver:	n/a	n/a
6	CHD1	chr12:121341195-121341317	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:121341283-121341610	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr12:121341285-121341472	K562	blood:	n/a	n/a
9	CHD2	chr12:121341216-121341587	GM12878	blood:	n/a	n/a
10	CREB1	chr12:121341075-121342607	GM12878	blood:	n/a	n/a
11	CREB1	chr12:121341159-121341507	A549	lung:	n/a	n/a
12	CTCF	chr12:121341480-121341630	GM12875	blood:	n/a	chr12:121341492-121341505
13	CTCF	chr12:121341420-121341570	GM12873	blood:	n/a	chr12:121341492-121341505
14	CTCF	chr12:121341440-121341590	GM12866	blood:	n/a	chr12:121341492-121341505
15	CTCF	chr12:121341400-121341550	HUVEC	blood vessel:	n/a	chr12:121341492-121341505
16	CTCF	chr12:121341381-121341443	GM19239	blood:	n/a	n/a
17	CTCF	chr12:121341380-121341530	GM12874	blood:	n/a	chr12:121341492-121341505
18	CTCF	chr12:121341446-121341502	GM19240	blood:	n/a	n/a
19	CTCF	chr12:121341420-121341570	GM12865	blood:	n/a	chr12:121341492-121341505
20	CTCF	chr12:121341423-121341458	GM10248	blood:	n/a	n/a
21	CTCF	chr12:121341345-121341507	GM12878	blood:	n/a	chr12:121341492-121341505
22	CTCF	chr12:121341455-121341556	GM12892	blood:	n/a	chr12:121341492-121341505
23	CTCF	chr12:121341400-121341550	GM06990	blood:	n/a	chr12:121341492-121341505
24	CTCF	chr12:121341454-121341579	GM19239	blood:	n/a	chr12:121341492-121341505
25	CTCF	chr12:121341460-121341610	GM12874	blood:	n/a	chr12:121341492-121341505
26	CTCF	chr12:121341320-121341470	GM12875	blood:	n/a	n/a
27	CTCF	chr12:121341360-121341510	GM12871	blood:	n/a	chr12:121341492-121341505
28	CTCF	chr12:121341466-121341483	GM10248	blood:	n/a	n/a
29	CTCF	chr12:121341460-121341610	GM12868	blood:	n/a	chr12:121341492-121341505
30	CTCF	chr12:121341460-121341610	GM12864	blood:	n/a	chr12:121341492-121341505
31	CTCF	chr12:121341460-121341610	GM12867	blood:	n/a	chr12:121341492-121341505
32	CTCF	chr12:121341454-121341509	GM10266	blood:	n/a	chr12:121341492-121341505
33	CTCF	chr12:121341410-121341560	GM19238	blood:	n/a	chr12:121341492-121341505
34	E2F4	chr12:121340495-121340599	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F6	chr12:121341293-121341445	K562	blood:	n/a	n/a
36	EBF1	chr12:121341250-121341415	GM12878	blood:	n/a	n/a
37	EGR1	chr12:121341133-121341580	K562	blood:	n/a	chr12:121341537-121341547 chr12:121341350-121341364 chr12:121341490-121341500 chr12:121341535-121341545 chr12:121341531-121341541 chr12:121341489-121341499 chr12:121341532-121341545 chr12:121341476-121341485 chr12:121341489-121341502
38	EGR1	chr12:121341208-121341558	K562	blood:	n/a	chr12:121341537-121341547 chr12:121341350-121341364 chr12:121341490-121341500 chr12:121341535-121341545 chr12:121341531-121341541 chr12:121341489-121341499 chr12:121341532-121341545 chr12:121341476-121341485 chr12:121341489-121341502
39	EGR1	chr12:121341180-121341563	GM12878	blood:	n/a	chr12:121341537-121341547 chr12:121341350-121341364 chr12:121341490-121341500 chr12:121341535-121341545 chr12:121341531-121341541 chr12:121341489-121341499 chr12:121341532-121341545 chr12:121341476-121341485 chr12:121341489-121341502
40	ELF1	chr12:121341192-121341498	HepG2	liver:	n/a	n/a
41	ELF1	chr12:121341132-121341471	HepG2	liver:	n/a	n/a
42	ELF1	chr12:121341126-121341502	K562	blood:	n/a	n/a
43	ELF1	chr12:121340976-121341881	GM12878	blood:	n/a	chr12:121341102-121341114
44	ELF1	chr12:121341031-121341571	K562	blood:	n/a	chr12:121341102-121341114
45	ELF1	chr12:121341035-121341514	MCF-7	breast:	n/a	chr12:121341102-121341114
46	ELF1	chr12:121341079-121341606	GM12878	blood:	n/a	chr12:121341102-121341114
47	EP300	chr12:121341197-121342606	SK-N-SH	brain:	n/a	chr12:121341955-121341971 chr12:121341953-121341962 chr12:121341913-121341922 chr12:121341910-121341919 chr12:121341956-121341965 chr12:121341916-121341925 chr12:121342327-121342343
48	EP300	chr12:121341279-121341398	HepG2	liver:	n/a	n/a
49	EP300	chr12:121340424-121340611	K562	blood:	n/a	n/a
50	FOS	chr12:121341338-121341389	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121341326-121341376	AG04449	skin:	fetal
2	chr12:121341326-121341376	NHBE	bronchial:	n/a
3	chr12:121341326-121341376	HUVEC	blood vessel:	n/a
4	chr12:121341326-121341376	AG10803	skin:	n/a
5	chr12:121341326-121341376	PANC-1	pancreas:	n/a
6	chr12:121341326-121341376	NH-A	brain:	n/a
7	chr12:121341326-121341376	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:121341326-121341376	NHDF-neo	bronchial:	n/a
9	chr12:121341326-121341376	Hela-S3	cervix:	n/a
10	chr12:121341326-121341376	U87	brain:	n/a
11	chr12:121341326-121341376	HepG2	liver:	n/a
12	chr12:121341326-121341376	HRPEpiC	eye:	n/a
13	chr12:121341326-121341376	CMK	blood:	n/a
14	chr12:121341326-121341376	BE2_C	brain:	n/a
15	chr12:121341326-121341376	ECC-1	luminal epithelium:	n/a
16	chr12:121341326-121341376	GM19239	blood:	n/a
17	chr12:121341326-121341376	GM06990	blood:	n/a
18	chr12:121341326-121341376	AoSMC	blood vessel:	n/a
19	chr12:121341326-121341376	SK-N-SH	brain:	n/a
20	chr12:121341326-121341376	SAEC	small airway:	n/a
21	chr12:121341326-121341376	T-47D	breast:	n/a
22	chr12:121341326-121341376	BJ	skin:	n/a
23	chr12:121341326-121341376	HCF	heart:	n/a
24	chr12:121341326-121341376	HMEC	breast:	n/a
25	chr12:121341326-121341376	H1-hESC	embryonic stem cell:	embryo
26	chr12:121341326-121341376	Hepatocyte	liver:	n/a
27	chr12:121341326-121341376	HCM	heart:	n/a
28	chr12:121341326-121341376	IMR90	lung:	fetal
29	chr12:121341326-121341376	AG09319	gingival:	n/a
30	chr12:121341326-121341376	HCPEpiC	choroid plexus:	n/a
31	chr12:121341326-121341376	ProgFib	skin:	n/a
32	chr12:121341326-121341376	LNCaP	prostate:	n/a
33	chr12:121341326-121341376	HAEpiC	amniotic membrane:	n/a
34	chr12:121341326-121341376	GM12891	blood:	n/a
35	chr12:121341326-121341376	MCF10A-Er-Src	breast:	n/a
36	chr12:121341326-121341376	HRE	kidney:	n/a
37	chr12:121341326-121341376	K562	blood:	n/a
38	chr12:121341326-121341376	MCF-7	breast:	n/a
39	chr12:121341326-121341376	PrEC	prostate:	n/a
40	chr12:121341326-121341376	HCT-116	colon:	n/a
41	chr12:121341326-121341376	SK-N-SH_RA	brain:	n/a
42	chr12:121341326-121341376	AG09309	skin:	n/a
43	chr12:121341326-121341376	RPTEC	kidney:	n/a
44	chr12:121341326-121341376	NB4	blood:	n/a
45	chr12:121341326-121341376	NT2-D1	testis:	n/a
46	chr12:121341326-121341376	HIPEpiC	eye:	n/a
47	chr12:121341326-121341376	HEEpiC	esophagus:	n/a
48	chr12:121341326-121341376	HNPCEpiC	eye:	n/a
49	chr12:121341326-121341376	HL-60	blood:	n/a
50	chr12:121341326-121341376	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:121338472..121340356-chr12:121340571..121343275,2	MCF-7	breast:

Variant related genes	Relation type
SPPL3	TF binding region
SPPL3	CpG island
ENSG00000157837	chromatin interactions

Extended variants
information (count: 57 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs869781	chr12:121340246-121340247	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536162501	chr12:121340277-121340278	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143584184	chr12:121340291-121340292	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569762194	chr12:121340302-121340303	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1151850	chr12:121340363-121340364	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs113365487	chr12:121340364-121340365	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558415242	chr12:121340370-121340371	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572161717	chr12:121340401-121340402	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs541065468	chr12:121340412-121340413	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs554585708	chr12:121340418-121340419	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs73224306	chr12:121340428-121340429	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542969425	chr12:121340431-121340432	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs563149023	chr12:121340443-121340444	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs531855466	chr12:121340471-121340472	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs545571356	chr12:121340552-121340553	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs118055784	chr12:121340571-121340572	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs147170362	chr12:121340586-121340587	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs547458094	chr12:121340597-121340598	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs1151849	chr12:121340599-121340600	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs189618723	chr12:121340660-121340661	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs183398884	chr12:121340695-121340696	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs75922909	chr12:121340745-121340746	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs117679209	chr12:121340749-121340750	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs148212637	chr12:121340794-121340795	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs1105416	chr12:121340799-121340800	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs569861593	chr12:121340800-121340801	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs186316405	chr12:121340854-121340855	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548575663	chr12:121340857-121340858	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs190779259	chr12:121340884-121340885	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574497146	chr12:121341001-121341002	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs537045475	chr12:121341056-121341057	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs558973347	chr12:121341057-121341058	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs187106561	chr12:121341071-121341072	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs192880393	chr12:121341073-121341074	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs113992016	chr12:121341075-121341076	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372377400	chr12:121341076-121341077	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs533019583	chr12:121341080-121341081	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs71076682	chr12:121341081-121341082	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs545300771	chr12:121341138-121341139	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs142765995	chr12:121341149-121341150	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184601122	chr12:121341155-121341156	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs565158627	chr12:121341158-121341159	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200351307	chr12:121341164-121341165	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs71076683	chr12:121341165-121341166	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs66511068	chr12:121341166-121341167	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs188740117	chr12:121341171-121341172	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs541134794	chr12:121341193-121341194	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561001457	chr12:121341196-121341197	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530087844	chr12:121341197-121341198	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs376240740	chr12:121341199-121341200	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121294200-121340400	Weak transcription	HSMM	muscle
2	chr12:121318200-121340400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr12:121323600-121340600	Weak transcription	Aorta	Aorta
4	chr12:121324000-121340400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:121329000-121340400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:121332000-121340600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:121332400-121340600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:121333200-121340400	Weak transcription	Gastric	stomach
9	chr12:121335800-121340400	Weak transcription	NH-A	brain
10	chr12:121338000-121340600	Enhancers	Small Intestine	intestine
11	chr12:121338200-121340400	Weak transcription	Placenta	Placenta
12	chr12:121338200-121340600	Enhancers	Primary T cells fromperipheralblood	blood
13	chr12:121338400-121340400	Weak transcription	Esophagus	oesophagus
14	chr12:121338400-121340400	Weak transcription	Lung	lung
15	chr12:121338400-121340600	Enhancers	Primary B cells from peripheral blood	blood
16	chr12:121338600-121340400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:121338600-121340400	Weak transcription	Thymus	Thymus
18	chr12:121338800-121340600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr12:121339400-121340400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:121339400-121340600	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr12:121339400-121340600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:121339400-121340600	Flanking Active TSS	GM12878-XiMat	blood
23	chr12:121339400-121341200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr12:121339600-121340400	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr12:121339600-121340400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr12:121339600-121340400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr12:121339600-121340400	Enhancers	Brain Angular Gyrus	brain
28	chr12:121339600-121340400	Enhancers	Brain Substantia Nigra	brain
29	chr12:121339600-121340400	Genic enhancers	Fetal Muscle Leg	muscle
30	chr12:121339600-121340400	Enhancers	Right Ventricle	heart
31	chr12:121339600-121340400	Enhancers	HepG2	liver
32	chr12:121339600-121340600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr12:121339600-121340600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr12:121339600-121340600	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr12:121339800-121340400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:121339800-121340400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr12:121339800-121340400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:121339800-121340400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:121339800-121340400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr12:121339800-121340400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:121339800-121340400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr12:121339800-121340400	Enhancers	Liver	Liver
43	chr12:121339800-121340400	Enhancers	Left Ventricle	heart
44	chr12:121339800-121340400	Enhancers	Psoas Muscle	Psoas
45	chr12:121339800-121340400	Active TSS	Right Atrium	heart
46	chr12:121339800-121340400	Enhancers	A549	lung
47	chr12:121339800-121340400	Enhancers	HSMMtube	muscle
48	chr12:121339800-121340600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:121339800-121340600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:121339800-121340600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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