Variant report

Variant	esv3437337
Chromosome Location	chr12:123872949-123874547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:565)
CpG islands
(count:305)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123872141-123873037	K562	blood:	n/a	n/a
2	ATF1	chr12:123872000-123873150	K562	blood:	n/a	n/a
3	ATF2	chr12:123872859-123873307	GM12878	blood:	n/a	n/a
4	BACH1	chr12:123872212-123873052	K562	blood:	n/a	n/a
5	BCLAF1	chr12:123872847-123873364	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:123872863-123873228	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:123873472-123873547	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:123871961-123873162	K562	blood:	n/a	n/a
9	BRCA1	chr12:123873103-123873374	GM12878	blood:	n/a	n/a
10	CBX3	chr12:123871927-123873272	K562	blood:	n/a	n/a
11	CBX3	chr12:123872436-123873022	K562	blood:	n/a	n/a
12	CCNT2	chr12:123872168-123874833	K562	blood:	n/a	n/a
13	CEBPB	chr12:123872099-123873143	K562	blood:	n/a	n/a
14	CEBPB	chr12:123872227-123873092	K562	blood:	n/a	n/a
15	CEBPB	chr12:123873220-123873222	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr12:123872026-123873173	K562	blood:	n/a	n/a
17	CEBPD	chr12:123873394-123873663	HepG2	liver:	n/a	n/a
18	CEBPD	chr12:123871766-123873277	K562	blood:	n/a	n/a
19	CHD1	chr12:123872993-123873125	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:123873357-123873383	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr12:123873155-123873536	HepG2	liver:	n/a	n/a
22	CHD2	chr12:123874289-123874302	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr12:123874352-123874413	GM12878	blood:	n/a	n/a
24	CHD2	chr12:123872308-123873529	K562	blood:	n/a	n/a
25	CHD2	chr12:123873190-123873649	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr12:123872906-123873570	GM12878	blood:	n/a	n/a
27	CREB1	chr12:123873022-123873718	A549	lung:	n/a	n/a
28	CREB1	chr12:123873952-123874248	A549	lung:	n/a	n/a
29	CTCF	chr12:123873359-123873680	K562	blood:	n/a	n/a
30	CTCF	chr12:123874300-123874450	BJ	skin:	n/a	n/a
31	CTCF	chr12:123874160-123874310	GM12873	blood:	n/a	n/a
32	CTCF	chr12:123874140-123874290	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr12:123873240-123873390	AG10803	skin:	n/a	n/a
34	CTCF	chr12:123873349-123873389	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:123873240-123873390	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr12:123874159-123874312	IMR90	lung:	n/a	n/a
37	CTCF	chr12:123873330-123873394	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr12:123873514-123873644	GM12892	blood:	n/a	n/a
39	CTCF	chr12:123874140-123874290	SAEC	small airway:	n/a	n/a
40	CTCF	chr12:123873250-123873435	HepG2	liver:	n/a	n/a
41	CTCF	chr12:123873260-123873410	GM12870	blood:	n/a	n/a
42	CTCF	chr12:123873240-123873390	GM12875	blood:	n/a	n/a
43	CTCF	chr12:123873540-123873690	GM12866	blood:	n/a	n/a
44	CTCF	chr12:123873460-123873610	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr12:123873520-123873670	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr12:123873354-123873454	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr12:123874160-123874310	HEK293	kidney:	n/a	n/a
48	CTCF	chr12:123873300-123873450	GM12864	blood:	n/a	n/a
49	CTCF	chr12:123874120-123874270	GM12873	blood:	n/a	n/a
50	CTCF	chr12:123873507-123873660	GM19239	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123874243-123874293	HEEpiC	esophagus:	n/a
2	chr12:123874298-123874348	HEK293	kidney:	embryo
3	chr12:123873524-123873574	BJ	skin:	n/a
4	chr12:123874456-123874506	SKMC	muscle:	n/a
5	chr12:123874243-123874293	ProgFib	skin:	n/a
6	chr12:123874298-123874348	Hela-S3	cervix:	n/a
7	chr12:123874243-123874293	ECC-1	luminal epithelium:	n/a
8	chr12:123874243-123874293	HCF	heart:	n/a
9	chr12:123874298-123874348	HIPEpiC	eye:	n/a
10	chr12:123874466-123874516	MCF10A-Er-Src	breast:	n/a
11	chr12:123874298-123874348	SK-N-MC	brain:	n/a
12	chr12:123874243-123874293	SK-N-MC	brain:	n/a
13	chr12:123874298-123874348	HRPEpiC	eye:	n/a
14	chr12:123873524-123873574	HUVEC	blood vessel:	n/a
15	chr12:123874456-123874506	AG09309	skin:	n/a
16	chr12:123874466-123874516	PFSK-1	brain:	n/a
17	chr12:123874243-123874293	NB4	blood:	n/a
18	chr12:123873524-123873574	HCM	heart:	n/a
19	chr12:123874298-123874348	A549	lung:	n/a
20	chr12:123874298-123874348	NH-A	brain:	n/a
21	chr12:123873524-123873574	SAEC	small airway:	n/a
22	chr12:123874466-123874516	HUVEC	blood vessel:	n/a
23	chr12:123874456-123874506	NHBE	bronchial:	n/a
24	chr12:123874243-123874293	HEK293	kidney:	embryo
25	chr12:123874298-123874348	HCF	heart:	n/a
26	chr12:123874456-123874506	IMR90	lung:	fetal
27	chr12:123874456-123874506	HCPEpiC	choroid plexus:	n/a
28	chr12:123874298-123874348	GM12892	blood:	n/a
29	chr12:123874243-123874293	U87	brain:	n/a
30	chr12:123873524-123873574	SK-N-SH_RA	brain:	n/a
31	chr12:123874466-123874516	GM19239	blood:	n/a
32	chr12:123874243-123874293	HepG2	liver:	n/a
33	chr12:123873524-123873574	HEK293	kidney:	embryo
34	chr12:123874466-123874516	BE2_C	brain:	n/a
35	chr12:123874466-123874516	AG09309	skin:	n/a
36	chr12:123874456-123874506	AoSMC	blood vessel:	n/a
37	chr12:123873524-123873574	SKMC	muscle:	n/a
38	chr12:123874298-123874348	GM19239	blood:	n/a
39	chr12:123874298-123874348	HCPEpiC	choroid plexus:	n/a
40	chr12:123873524-123873574	ProgFib	skin:	n/a
41	chr12:123874466-123874516	HCF	heart:	n/a
42	chr12:123874466-123874516	SK-N-SH_RA	brain:	n/a
43	chr12:123874456-123874506	A549	lung:	n/a
44	chr12:123874243-123874293	HL-60	blood:	n/a
45	chr12:123873524-123873574	AG04449	skin:	fetal
46	chr12:123873524-123873574	NHDF-neo	bronchial:	n/a
47	chr12:123874298-123874348	Caco-2	colon:	n/a
48	chr12:123874466-123874516	Hela-S3	cervix:	n/a
49	chr12:123874466-123874516	HCM	heart:	n/a
50	chr12:123873524-123873574	HCT-116	colon:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123717467..123721119-chr12:123869942..123873013,3	K562	blood:
2	chr12:123753349..123756927-chr12:123873006..123875020,4	MCF-7	breast:
3	chr12:123847204..123849398-chr12:123874460..123876425,2	K562	blood:
4	chr12:123872765..123874584-chr2:91935567..91938569,3	MCF-7	breast:
5	chr12:123871385..123875741-chr12:124017374..124019532,6	MCF-7	breast:
6	chr12:123872784..123874602-chr17:59484787..59486930,2	MCF-7	breast:
7	chr12:123872056..123874942-chr12:124085224..124088307,3	MCF-7	breast:
8	chr12:123870684..123873491-chr12:123941342..123943069,2	MCF-7	breast:
9	chr12:123753572..123756952-chr12:123872035..123874712,3	MCF-7	breast:
10	chr12:123872355..123875545-chr12:123919640..123922793,3	MCF-7	breast:
11	chr12:123754082..123756520-chr12:123873506..123875645,3	K562	blood:
12	chr11:45825943..45826929-chr12:123873071..123873715,2	Hela-S3	cervix:
13	chr12:123755164..123758333-chr12:123868507..123873426,5	K562	blood:
14	chr12:123715746..123718967-chr12:123870796..123875270,4	K562	blood:
15	chr12:123872778..123876196-chr12:124065295..124071344,6	MCF-7	breast:
16	chr12:123872223..123875553-chr12:124085591..124088201,3	MCF-7	breast:
17	chr12:123871220..123873431-chr12:123897619..123900288,2	K562	blood:
18	chr12:123845329..123854937-chr12:123865496..123876607,58	K562	blood:
19	chr12:123873719..123876506-chr12:124067448..124069174,2	K562	blood:
20	chr12:123873193..123874940-chr12:123942406..123944140,2	K562	blood:
21	chr12:123872416..123876102-chr12:124017252..124019601,4	MCF-7	breast:
22	chr12:123845591..123852236-chr12:123866929..123875043,19	MCF-7	breast:
23	chr12:123846590..123852305-chr12:123861449..123873718,39	K562	blood:
24	chr12:123871392..123873266-chr12:123879118..123880787,2	K562	blood:
25	chr12:123873866..123876385-chr12:123942538..123944226,2	MCF-7	breast:
26	chr12:123753478..123757222-chr12:123871925..123875006,5	K562	blood:
27	chr12:123870366..123875219-chr12:124064500..124069174,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNRNP35-4	chr12:123872989-123873304	NONHSAT031588

No data

Variant related genes	Relation type
SETD8	TF binding region
SETD8	CpG island
ENSG00000121068	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000232531	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000150977	chromatin interactions
ENSG00000051825	chromatin interactions

Extended variants
information (count: 28 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557021865	chr12:123873042-123873043	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
2	rs575862342	chr12:123873043-123873044	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
3	rs543626298	chr12:123873125-123873126	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
4	rs555239588	chr12:123873134-123873135	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
5	rs573889443	chr12:123873173-123873174	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
6	rs369997654	chr12:123873202-123873203	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
7	rs559438245	chr12:123873204-123873205	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
8	rs532948035	chr12:123873205-123873206	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
9	rs567772427	chr12:123873208-123873209	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
10	rs28533432	chr12:123873242-123873243	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs563393017	chr12:123873254-123873255	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
12	rs530488294	chr12:123873295-123873296	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
13	rs528195473	chr12:123873311-123873312	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs549562548	chr12:123873315-123873316	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs567705664	chr12:123873886-123873887	Weak transcription Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs112525458	chr12:123874000-123874001	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs186822980	chr12:123874034-123874035	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs528826116	chr12:123874271-123874272	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs546878122	chr12:123874272-123874273	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs553628309	chr12:123874288-123874289	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs538629612	chr12:123874361-123874362	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs377314405	chr12:123874371-123874372	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs191388726	chr12:123874407-123874408	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs370931623	chr12:123874410-123874411	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs28438946	chr12:123874423-123874424	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs374749850	chr12:123874430-123874431	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs536310553	chr12:123874469-123874470	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs555542202	chr12:123874480-123874481	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	14 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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123869600-123873000	Weak transcription	Aorta	Aorta
2	chr12:123872000-123873000	Flanking Active TSS	HepG2	liver
3	chr12:123872000-123873000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr12:123872000-123873200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr12:123872000-123873200	Flanking Active TSS	Dnd41	blood
6	chr12:123872200-123873000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:123872200-123873000	Enhancers	Gastric	stomach
8	chr12:123872200-123873000	Enhancers	Lung	lung
9	chr12:123872200-123873200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr12:123872200-123873200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr12:123872200-123873200	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr12:123872200-123873200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr12:123872200-123873200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:123872200-123873200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr12:123872200-123873200	Flanking Active TSS	Fetal Brain Male	brain
16	chr12:123872200-123873200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
17	chr12:123872200-123873200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr12:123872200-123873200	Flanking Active TSS	Hela-S3	cervix
19	chr12:123872400-123873000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:123872400-123873000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:123872400-123873000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
22	chr12:123872400-123873000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:123872400-123873000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:123872400-123873000	Flanking Active TSS	Fetal Heart	heart
25	chr12:123872400-123873000	Flanking Active TSS	Rectal Smooth Muscle	rectum
26	chr12:123872400-123873000	Flanking Active TSS	A549	lung
27	chr12:123872400-123873000	Transcr. at gene 5' and 3'	NHEK	skin
28	chr12:123872400-123873200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr12:123872400-123873200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:123872400-123873200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:123872400-123873200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:123872400-123873200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:123872400-123873200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:123872400-123873200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:123872400-123873200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:123872400-123873200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr12:123872400-123873200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr12:123872400-123873200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr12:123872400-123873200	Flanking Active TSS	Fetal Intestine Small	intestine
40	chr12:123872400-123873200	Flanking Active TSS	Fetal Thymus	thymus
41	chr12:123872400-123873200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr12:123872400-123873200	Flanking Active TSS	HMEC	breast
43	chr12:123872600-123873000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr12:123872600-123873000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:123872600-123873000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:123872600-123873000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
47	chr12:123872600-123873000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
48	chr12:123872600-123873000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr12:123872600-123873000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr12:123872600-123873000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

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