Variant report

Variant	esv13410
Chromosome Location	chr12:124017022-124017617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:145)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:145 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124017367-124017624	K562	blood:	n/a	n/a
2	BCLAF1	chr12:124016596-124017027	GM12878	blood:	n/a	chr12:124016835-124016844
3	BHLHE40	chr12:124017508-124017986	HepG2	liver:	n/a	chr12:124017636-124017652
4	BHLHE40	chr12:124017548-124018031	GM12878	blood:	n/a	chr12:124017636-124017652
5	BHLHE40	chr12:124017420-124018105	K562	blood:	n/a	chr12:124017636-124017652
6	BRCA1	chr12:124017418-124017970	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr12:124017259-124018108	K562	blood:	n/a	n/a
8	CCNT2	chr12:124017594-124018993	K562	blood:	n/a	chr12:124018745-124018754
9	CEBPB	chr12:124017334-124018091	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr12:124017413-124018001	K562	blood:	n/a	n/a
11	CREB1	chr12:124017568-124018148	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr12:124017473-124018163	A549	lung:	n/a	n/a
13	CUX1	chr12:124017425-124017512	K562	blood:	n/a	n/a
14	E2F6	chr12:124017518-124018305	A549	lung:	n/a	n/a
15	E2F6	chr12:124017474-124018601	K562	blood:	n/a	chr12:124018461-124018468 chr12:124018312-124018321 chr12:124018465-124018475 chr12:124018468-124018478
16	E2F6	chr12:124017443-124018183	A549	lung:	n/a	n/a
17	E2F6	chr12:124017560-124018651	K562	blood:	n/a	chr12:124018461-124018468 chr12:124018312-124018321 chr12:124018465-124018475 chr12:124018468-124018478
18	E2F6	chr12:124017502-124018246	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F6	chr12:124017363-124018308	H1-hESC	embryonic stem cell:	n/a	n/a
20	EGR1	chr12:124017580-124017849	K562	blood:	n/a	n/a
21	EGR1	chr12:124017510-124017888	K562	blood:	n/a	n/a
22	ELF1	chr12:124017324-124017932	A549	lung:	n/a	chr12:124017651-124017664
23	ELF1	chr12:124017440-124017865	K562	blood:	n/a	chr12:124017651-124017664
24	ELF1	chr12:124017322-124017956	A549	lung:	n/a	chr12:124017651-124017664
25	ELF1	chr12:124017385-124018213	MCF-7	breast:	n/a	chr12:124017651-124017664
26	ELF1	chr12:124017437-124017831	HepG2	liver:	n/a	chr12:124017651-124017664
27	ELF1	chr12:124017443-124017964	GM12878	blood:	n/a	chr12:124017651-124017664
28	ELF1	chr12:124017362-124017936	K562	blood:	n/a	chr12:124017651-124017664
29	ELF1	chr12:124017480-124017784	HepG2	liver:	n/a	chr12:124017651-124017664
30	EP300	chr12:124017388-124017540	K562	blood:	n/a	n/a
31	GABPA	chr12:124017543-124017917	K562	blood:	n/a	chr12:124017630-124017639
32	HCFC1	chr12:124017502-124018095	K562	blood:	n/a	n/a
33	HDAC2	chr12:124017608-124018022	HepG2	liver:	n/a	n/a
34	HEY1	chr12:124017522-124018136	K562	blood:	n/a	n/a
35	HEY1	chr12:124017561-124019062	HepG2	liver:	n/a	chr12:124018509-124018524
36	HMGN3	chr12:124017509-124019090	K562	blood:	n/a	n/a
37	IRF4	chr12:124016529-124017044	GM12878	blood:	n/a	n/a
38	MAFK	chr12:124017321-124017328	K562	blood:	n/a	n/a
39	MAFK	chr12:124017475-124017763	Hela-S3	cervix:	n/a	n/a
40	MAX	chr12:124017452-124018226	ECC-1	luminal epithelium:	n/a	chr12:124017624-124017639
41	MAX	chr12:124017446-124019193	K562	blood:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
42	MAX	chr12:124017423-124018547	MCF-7	breast:	n/a	chr12:124017624-124017639
43	MAX	chr12:124017421-124018127	K562	blood:	n/a	chr12:124017624-124017639
44	MAX	chr12:124017515-124018571	ECC-1	luminal epithelium:	n/a	chr12:124017624-124017639
45	MAX	chr12:124017425-124018291	H1-hESC	embryonic stem cell:	n/a	chr12:124017624-124017639
46	MAX	chr12:124017309-124019259	HepG2	liver:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
47	MAX	chr12:124017459-124018605	Hela-S3	cervix:	n/a	chr12:124017624-124017639
48	MAX	chr12:124017255-124019402	A549	lung:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
49	MAX	chr12:124017269-124019274	A549	lung:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
50	MAX	chr12:124017437-124018147	SK-N-SH	brain:	n/a	chr12:124017624-124017639

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124017613-124017663	HRPEpiC	eye:	n/a
2	chr12:124017613-124017663	HepG2	liver:	n/a
3	chr12:124017613-124017663	HL-60	blood:	n/a
4	chr12:124017613-124017663	A549	lung:	n/a
5	chr12:124017613-124017663	GM19239	blood:	n/a
6	chr12:124017613-124017663	GM12878	blood:	n/a
7	chr12:124017613-124017663	BE2_C	brain:	n/a
8	chr12:124017613-124017663	HUVEC	blood vessel:	n/a
9	chr12:124017613-124017663	SAEC	small airway:	n/a
10	chr12:124017613-124017663	RPTEC	kidney:	n/a
11	chr12:124017613-124017663	HCF	heart:	n/a
12	chr12:124017613-124017663	IMR90	lung:	fetal
13	chr12:124017613-124017663	AG04450	lung:	fetal
14	chr12:124017613-124017663	HCM	heart:	n/a
15	chr12:124017613-124017663	AG09309	skin:	n/a
16	chr12:124017613-124017663	SKMC	muscle:	n/a
17	chr12:124017613-124017663	HCT-116	colon:	n/a
18	chr12:124017613-124017663	HRCEpiC	kidney:	n/a
19	chr12:124017613-124017663	GM12891	blood:	n/a
20	chr12:124017613-124017663	BJ	skin:	n/a
21	chr12:124017613-124017663	PANC-1	pancreas:	n/a
22	chr12:124017613-124017663	PrEC	prostate:	n/a
23	chr12:124017613-124017663	NH-A	brain:	n/a
24	chr12:124017613-124017663	Hela-S3	cervix:	n/a
25	chr12:124017613-124017663	SK-N-SH	brain:	n/a
26	chr12:124017613-124017663	HEEpiC	esophagus:	n/a
27	chr12:124017613-124017663	U87	brain:	n/a
28	chr12:124017613-124017663	Caco-2	colon:	n/a
29	chr12:124017613-124017663	ProgFib	skin:	n/a
30	chr12:124017613-124017663	HAEpiC	amniotic membrane:	n/a
31	chr12:124017613-124017663	AG04449	skin:	fetal
32	chr12:124017613-124017663	HNPCEpiC	eye:	n/a
33	chr12:124017613-124017663	T-47D	breast:	n/a
34	chr12:124017613-124017663	HCPEpiC	choroid plexus:	n/a
35	chr12:124017613-124017663	SK-N-MC	brain:	n/a
36	chr12:124017613-124017663	LNCaP	prostate:	n/a
37	chr12:124017613-124017663	AG09319	gingival:	n/a
38	chr12:124017613-124017663	HEK293	kidney:	embryo
39	chr12:124017613-124017663	HRE	kidney:	n/a
40	chr12:124017613-124017663	AG10803	skin:	n/a
41	chr12:124017613-124017663	NB4	blood:	n/a
42	chr12:124017613-124017663	NHDF-neo	bronchial:	n/a
43	chr12:124017613-124017663	Hepatocyte	liver:	n/a
44	chr12:124017613-124017663	Jurkat	blood:	n/a
45	chr12:124017613-124017663	GM12892	blood:	n/a
46	chr12:124017613-124017663	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:124017613-124017663	HMEC	breast:	n/a
48	chr12:124017613-124017663	ovcar-3	ovarian:	n/a
49	chr12:124017613-124017663	CMK	blood:	n/a
50	chr12:124017613-124017663	PFSK-1	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123998884..124001416-chr12:124016546..124018370,2	K562	blood:
2	chr12:123872416..123876102-chr12:124017252..124019601,4	MCF-7	breast:
3	chr12:123948940..123951509-chr12:124017235..124019368,2	MCF-7	breast:
4	chr12:123873494..123875550-chr12:124015653..124017169,2	MCF-7	breast:
5	chr12:124015786..124020200-chr12:124020787..124024805,6	K562	blood:
6	chr12:124016749..124018606-chr12:124069216..124071514,2	K562	blood:
7	chr12:123753293..123757508-chr12:124015727..124020202,5	K562	blood:
8	chr12:124017444..124019100-chr12:124084646..124086674,2	MCF-7	breast:
9	chr12:123943032..123944561-chr12:124016969..124018583,2	MCF-7	breast:
10	chr12:123942564..123944577-chr12:124016063..124019666,4	MCF-7	breast:
11	chr12:123871385..123875741-chr12:124017374..124019532,6	MCF-7	breast:
12	chr12:124006455..124008310-chr12:124016022..124017705,2	K562	blood:
13	chr12:124015709..124018064-chr12:124066858..124069100,3	MCF-7	breast:
14	chr12:123997284..124000079-chr12:124017073..124019484,2	MCF-7	breast:
15	chr12:123947470..123950375-chr12:124015636..124018854,3	K562	blood:

No data

Variant related genes	Relation type
MIR3908	TF binding region
MIR3908	CpG island
ENSG00000188026	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000266655	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000086598	chromatin interactions

Extended variants
information (count: 27 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528247634	chr12:124017059-124017060	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs143480607	chr12:124017079-124017080	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs536252540	chr12:124017099-124017100	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs145450506	chr12:124017108-124017109	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs377231050	chr12:124017116-124017117	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs140254380	chr12:124017128-124017129	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs546636358	chr12:124017153-124017154	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs184541763	chr12:124017164-124017165	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs201212484	chr12:124017205-124017206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs371925078	chr12:124017250-124017251	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs576686917	chr12:124017252-124017253	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs71458805	chr12:124017254-124017255	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs72498677	chr12:124017256-124017257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs536369840	chr12:124017258-124017259	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs375142298	chr12:124017262-124017263	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs11442373	chr12:124017301-124017302	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs548829590	chr12:124017317-124017318	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs190640711	chr12:124017402-124017403	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs180843715	chr12:124017403-124017404	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs534384578	chr12:124017428-124017429	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs559341130	chr12:124017484-124017485	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs577619299	chr12:124017485-124017486	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs369103333	chr12:124017506-124017507	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs538501708	chr12:124017515-124017516	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs35866415	chr12:124017568-124017569	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs28478308	chr12:124017569-124017570	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs542335189	chr12:124017585-124017586	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124001200-124017400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:124001400-124017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:124006200-124017600	Weak transcription	Small Intestine	intestine
4	chr12:124007800-124017400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:124008000-124017400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:124008200-124017200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr12:124008400-124017400	Weak transcription	Gastric	stomach
8	chr12:124015200-124017200	Genic enhancers	Fetal Stomach	stomach
9	chr12:124015200-124017400	Enhancers	Pancreas	Pancrea
10	chr12:124015400-124018000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr12:124015800-124017200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:124015800-124017200	Genic enhancers	Fetal Muscle Trunk	muscle
13	chr12:124015800-124017400	Enhancers	Esophagus	oesophagus
14	chr12:124016000-124017400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
15	chr12:124016000-124017400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr12:124016000-124017400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr12:124016000-124017400	Enhancers	Fetal Lung	lung
18	chr12:124016000-124017600	Flanking Active TSS	Brain Substantia Nigra	brain
19	chr12:124016200-124017200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:124016200-124017400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr12:124016200-124017800	Flanking Active TSS	HUVEC	blood vessel
22	chr12:124016200-124018000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr12:124016400-124017200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr12:124016400-124017200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:124016400-124017200	Flanking Active TSS	Colon Smooth Muscle	Colon
26	chr12:124016400-124017200	Flanking Active TSS	Hela-S3	cervix
27	chr12:124016400-124017400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr12:124016400-124017400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr12:124016400-124017400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:124016400-124017400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr12:124016400-124017400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:124016400-124017400	Enhancers	Liver	Liver
33	chr12:124016400-124017400	Flanking Active TSS	Brain Angular Gyrus	brain
34	chr12:124016400-124017400	Enhancers	Colonic Mucosa	Colon
35	chr12:124016400-124017400	Enhancers	Duodenum Mucosa	Duodenum
36	chr12:124016400-124017400	Enhancers	Fetal Intestine Large	intestine
37	chr12:124016400-124017600	Enhancers	Primary B cells from peripheral blood	blood
38	chr12:124016400-124017600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr12:124016400-124017600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr12:124016400-124017600	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr12:124016400-124017600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr12:124016400-124017600	Bivalent Enhancer	Fetal Thymus	thymus
43	chr12:124016400-124017600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr12:124016400-124017600	Enhancers	Spleen	Spleen
45	chr12:124016400-124017600	Flanking Active TSS	Osteobl	bone
46	chr12:124016400-124018000	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr12:124016400-124018000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr12:124016400-124018000	Flanking Active TSS	HMEC	breast
49	chr12:124016400-124019400	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr12:124016600-124017200	Flanking Active TSS	Brain Anterior Caudate	brain

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