Variant report

Variant	nsv469473
Chromosome Location	chr12:74676381-74712896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:550)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74677511-74677734	K562	blood:	n/a	n/a
2	ARID3A	chr12:74686394-74686740	K562	blood:	n/a	n/a
3	ATF1	chr12:74686375-74686953	K562	blood:	n/a	n/a
4	ATF1	chr12:74706672-74706735	K562	blood:	n/a	n/a
5	BHLHE40	chr12:74687322-74688058	K562	blood:	n/a	n/a
6	BHLHE40	chr12:74686194-74687073	K562	blood:	n/a	n/a
7	CBX3	chr12:74686218-74687007	K562	blood:	n/a	n/a
8	CBX3	chr12:74686301-74686730	K562	blood:	n/a	n/a
9	CBX3	chr12:74687157-74687922	K562	blood:	n/a	n/a
10	CCNT2	chr12:74686228-74686909	K562	blood:	n/a	chr12:74686489-74686509
11	CEBPB	chr12:74686352-74686893	K562	blood:	n/a	n/a
12	CEBPB	chr12:74680258-74680372	K562	blood:	n/a	n/a
13	CEBPB	chr12:74686227-74686696	K562	blood:	n/a	n/a
14	CEBPB	chr12:74679616-74679818	A549	lung:	n/a	n/a
15	CEBPD	chr12:74686172-74686749	K562	blood:	n/a	n/a
16	CHD2	chr12:74686188-74686982	K562	blood:	n/a	n/a
17	CHD2	chr12:74687891-74688044	K562	blood:	n/a	n/a
18	CHD2	chr12:74687474-74687667	K562	blood:	n/a	n/a
19	CTCF	chr12:74710860-74711010	HEEpiC	esophagus:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
20	CTCF	chr12:74710820-74710970	HAc	cerebellar:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
21	CTCF	chr12:74710829-74711076	HepG2	liver:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
22	CTCF	chr12:74710780-74710930	HVMF	connective:	n/a	n/a
23	CTCF	chr12:74710880-74711030	HPF	lung:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
24	CTCF	chr12:74710940-74711090	HUVEC	blood vessel:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
25	CTCF	chr12:74710645-74711203	MCF-7	breast:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
26	CTCF	chr12:74710860-74711010	HRE	kidney:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
27	CTCF	chr12:74710774-74711156	H1-hESC	embryonic stem cell:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
28	CTCF	chr12:74686287-74686725	K562	blood:	n/a	chr12:74686694-74686707
29	CTCF	chr12:74710555-74711578	A549	lung:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
30	CTCF	chr12:74710980-74711130	HVMF	connective:	n/a	n/a
31	CTCF	chr12:74710860-74711010	HCFaa	heart:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
32	CTCF	chr12:74710880-74711030	K562	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
33	CTCF	chr12:74710862-74711056	Hela-S3	cervix:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
34	CTCF	chr12:74710900-74711050	HEEpiC	esophagus:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
35	CTCF	chr12:74710845-74711086	A549	lung:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
36	CTCF	chr12:74710920-74711070	GM12866	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
37	CTCF	chr12:74710932-74711012	GM13976	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
38	CTCF	chr12:74710880-74711030	Caco-2	colon:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
39	CTCF	chr12:74710880-74711030	HBMEC	blood vessel:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
40	CTCF	chr12:74686260-74686410	K562	blood:	n/a	n/a
41	CTCF	chr12:74710880-74711030	HCT-116	colon:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
42	CTCF	chr12:74710880-74711030	AG04449	skin:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
43	CTCF	chr12:74710940-74711090	BE2_C	brain:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
44	CTCF	chr12:74710740-74710890	GM12872	blood:	n/a	n/a
45	CTCF	chr12:74711040-74711190	A549	lung:	n/a	n/a
46	CTCF	chr12:74710900-74711050	AG04449	skin:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
47	CTCF	chr12:74710963-74711013	GM10266	blood:	n/a	n/a
48	CTCF	chr12:74710900-74711050	AoAF	blood vessel:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
49	CTCF	chr12:74710840-74710990	GM12867	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
50	CTCF	chr12:74710714-74711285	HCT-116	colon:	n/a	chr12:74710949-74710967 chr12:74710944-74710965

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74687807-74687857	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:74687807-74687857	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:74686430-74686480	SKMC	muscle:	n/a
4	chr12:74686282-74686332	ECC-1	luminal epithelium:	n/a
5	chr12:74687807-74687857	NB4	blood:	n/a
6	chr12:74686411-74686461	HCF	heart:	n/a
7	chr12:74687404-74687454	HIPEpiC	eye:	n/a
8	chr12:74686411-74686461	HIPEpiC	eye:	n/a
9	chr12:74686411-74686461	K562	blood:	n/a
10	chr12:74687404-74687454	GM19239	blood:	n/a
11	chr12:74686423-74686473	HMEC	breast:	n/a
12	chr12:74688000-74688050	LNCaP	prostate:	n/a
13	chr12:74686411-74686461	Jurkat	blood:	n/a
14	chr12:74687404-74687454	SK-N-SH_RA	brain:	n/a
15	chr12:74686367-74686417	HRPEpiC	eye:	n/a
16	chr12:74686430-74686480	HNPCEpiC	eye:	n/a
17	chr12:74687807-74687857	AG09309	skin:	n/a
18	chr12:74687404-74687454	GM12892	blood:	n/a
19	chr12:74686411-74686461	AG04450	lung:	fetal
20	chr12:74687807-74687857	HCT-116	colon:	n/a
21	chr12:74686282-74686332	HUVEC	blood vessel:	n/a
22	chr12:74686367-74686417	NB4	blood:	n/a
23	chr12:74686411-74686461	HEK293	kidney:	embryo
24	chr12:74687852-74687902	H1-hESC	embryonic stem cell:	embryo
25	chr12:74688000-74688050	AG09309	skin:	n/a
26	chr12:74688000-74688050	GM12892	blood:	n/a
27	chr12:74686411-74686461	SK-N-SH	brain:	n/a
28	chr12:74687852-74687902	AG04449	skin:	fetal
29	chr12:74686430-74686480	GM12891	blood:	n/a
30	chr12:74687404-74687454	HAEpiC	amniotic membrane:	n/a
31	chr12:74686411-74686461	HCPEpiC	choroid plexus:	n/a
32	chr12:74687404-74687454	HRCEpiC	kidney:	n/a
33	chr12:74686367-74686417	A549	lung:	n/a
34	chr12:74686411-74686461	MCF-7	breast:	n/a
35	chr12:74686282-74686332	HRPEpiC	eye:	n/a
36	chr12:74686282-74686332	NHBE	bronchial:	n/a
37	chr12:74686282-74686332	GM12891	blood:	n/a
38	chr12:74687807-74687857	HMEC	breast:	n/a
39	chr12:74686367-74686417	HCT-116	colon:	n/a
40	chr12:74686411-74686461	NHBE	bronchial:	n/a
41	chr12:74687404-74687454	HCT-116	colon:	n/a
42	chr12:74687852-74687902	CMK	blood:	n/a
43	chr12:74687404-74687454	GM12891	blood:	n/a
44	chr12:74686411-74686461	HAEpiC	amniotic membrane:	n/a
45	chr12:74687852-74687902	SKMC	muscle:	n/a
46	chr12:74686411-74686461	HCM	heart:	n/a
47	chr12:74687852-74687902	AoSMC	blood vessel:	n/a
48	chr12:74686282-74686332	T-47D	breast:	n/a
49	chr12:74686430-74686480	HCF	heart:	n/a
50	chr12:74686411-74686461	GM12878	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74697259..74699490-chr12:74701397..74704397,3	K562	blood:
2	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:
3	chr12:74505546..74506081-chr12:74710850..74711455,2	MCF-7	breast:
4	chr12:74685273..74687304-chrX:26574250..26577248,2	K562	blood:
5	chr12:74695518..74698139-chr12:74698904..74700700,2	MCF-7	breast:
6	chr12:74683740..74685933-chr12:74788608..74790315,2	K562	blood:
7	chr12:74415312..74416230-chr12:74710631..74711359,2	MCF-7	breast:
8	chr12:74710734..74711407-chr12:74759142..74759810,2	MCF-7	breast:
9	chr12:74687125..74689371-chr12:74929648..74931476,2	K562	blood:
10	chr12:74696546..74698313-chr12:74705755..74707980,2	K562	blood:
11	chr12:74563726..74565313-chr12:74683248..74684953,2	K562	blood:
12	chr12:74685342..74687615-chr12:74688335..74689861,2	K562	blood:
13	chr12:74686465..74688529-chr12:74932040..74934610,2	K562	blood:
14	chr12:74636496..74638215-chr12:74687391..74689120,2	K562	blood:
15	chr12:74682181..74684758-chr12:74690974..74692662,2	MCF-7	breast:
16	chr12:74690922..74693086-chr12:74695420..74697032,3	K562	blood:
17	chr12:74695518..74698139-chr12:74698904..74700700,2	MCF-7	breast:
18	chr12:74694041..74696981-chr12:74709470..74713007,3	K562	blood:
19	chr12:74700385..74702258-chr12:74705662..74707341,2	K562	blood:
20	chr12:74682181..74684758-chr12:74690974..74692662,2	MCF-7	breast:
21	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
22	chr12:74700385..74702258-chr12:74705662..74707341,2	K562	blood:
23	chr12:74697259..74699490-chr12:74701397..74704397,3	K562	blood:
24	chr12:74686333..74689178-chr12:74690372..74695495,6	K562	blood:
25	chr12:74690922..74693086-chr12:74695420..74697032,3	K562	blood:
26	chr12:74696546..74698313-chr12:74705755..74707980,2	K562	blood:
27	chr12:74694041..74696981-chr12:74709470..74713007,3	K562	blood:
28	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:
29	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-3	chr12:74677374-74677449	ENSG00000257183.1
2	lnc-KCNC2-2	chr12:74700338-74700449	ENSG00000251138
3	lnc-KCNC2-2	chr12:74678816-74678873	ENSG00000251138
4	lnc-KCNC2-2	chr12:74679640-74679726	ENSG00000251138
5	lnc-KCNC2-2	chr12:74686095-74686314	ENSG00000251138
6	lnc-KCNC2-2	chr12:74679478-74679726	ENSG00000251138

No data

Variant related genes	Relation type
ENSG00000251138	TF binding region
ENSG00000257183	TF binding region
ENSG00000257364	TF binding region
ENSG00000251138	CpG island
ENSG00000257183	CpG island
ENSG00000257364	CpG island
ENSG00000259849	chromatin interactions
ENSG00000257364	chromatin interactions
ENSG00000230265	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000251138	chromatin interactions
ENSG00000258320	chromatin interactions
PROSC	miRNA target sites
HOXC8	miRNA target sites
DYNLL2	miRNA target sites
DNMT1	miRNA target sites
RRAS	miRNA target sites

Extended variants
information (count: 829 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11180003	chr12:74676381-74676382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11180004	chr12:74676460-74676461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs151113043	chr12:74676539-74676540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556830906	chr12:74676632-74676633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186563884	chr12:74676665-74676666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536314657	chr12:74676674-74676675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572683247	chr12:74676689-74676690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79574361	chr12:74676729-74676730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573399291	chr12:74676794-74676795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545402479	chr12:74676797-74676798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565318058	chr12:74676807-74676808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375748008	chr12:74676820-74676821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576003778	chr12:74676861-74676862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191199371	chr12:74676881-74676882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561292245	chr12:74676965-74676966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530342081	chr12:74676966-74676967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546908624	chr12:74676969-74676970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559383540	chr12:74676971-74676972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149771616	chr12:74676983-74676984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550959834	chr12:74677012-74677013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184624019	chr12:74677048-74677049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190357342	chr12:74677088-74677089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550866738	chr12:74677156-74677157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574191053	chr12:74677191-74677192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193302421	chr12:74677202-74677203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536421427	chr12:74677237-74677238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184997373	chr12:74677254-74677255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566960370	chr12:74677334-74677335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574750632	chr12:74677363-74677364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539180670	chr12:74677369-74677370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558954042	chr12:74677381-74677382	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs145783206	chr12:74677382-74677383	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs141608771	chr12:74677456-74677457	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372857703	chr12:74677471-74677472	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534489753	chr12:74677472-74677473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575065429	chr12:74677516-74677517	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs11833117	chr12:74677518-74677519	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146984511	chr12:74677523-74677524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528130545	chr12:74677562-74677563	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs370267102	chr12:74677570-74677571	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs138086674	chr12:74677598-74677599	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189124097	chr12:74677617-74677618	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs530446074	chr12:74677663-74677664	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142153548	chr12:74677683-74677684	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs567534192	chr12:74677717-74677718	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs529982875	chr12:74677723-74677724	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs111239532	chr12:74677735-74677736	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73182767	chr12:74677747-74677748	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs61932953	chr12:74677790-74677791	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs559118255	chr12:74677836-74677837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74636600-74678000	Weak transcription	K562	blood
2	chr12:74676000-74679000	Weak transcription	HMEC	breast
3	chr12:74676200-74679200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:74678000-74678600	Genic enhancers	K562	blood
5	chr12:74678600-74678800	Strong transcription	K562	blood
6	chr12:74678800-74679400	Weak transcription	K562	blood
7	chr12:74679000-74679200	Enhancers	HMEC	breast
8	chr12:74679000-74679400	Enhancers	Placenta	Placenta
9	chr12:74679200-74679600	Weak transcription	HMEC	breast
10	chr12:74679200-74680000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:74679200-74680000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:74679200-74681400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:74679400-74680400	Enhancers	K562	blood
14	chr12:74679600-74680200	Enhancers	HMEC	breast
15	chr12:74679800-74680200	Enhancers	NHEK	skin
16	chr12:74680000-74680200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:74680000-74681000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:74680400-74680800	Weak transcription	K562	blood
19	chr12:74680800-74681000	Enhancers	K562	blood
20	chr12:74681000-74681200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:74681000-74681200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:74681000-74683600	Weak transcription	K562	blood
23	chr12:74681400-74690800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:74681800-74682200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr12:74681800-74683000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr12:74682000-74682400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:74682400-74682800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:74683000-74685600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:74683600-74684400	Enhancers	K562	blood
30	chr12:74684400-74684800	Flanking Active TSS	K562	blood
31	chr12:74684800-74686800	Active TSS	K562	blood
32	chr12:74685600-74688000	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr12:74686000-74687600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:74686200-74687000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr12:74686200-74688000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:74686400-74687800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr12:74686600-74687000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr12:74686600-74687000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:74686600-74689000	Weak transcription	Right Atrium	heart
40	chr12:74686800-74688000	Flanking Active TSS	K562	blood
41	chr12:74687600-74687800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:74687800-74688000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:74688000-74688200	Active TSS	K562	blood
44	chr12:74688200-74691800	Weak transcription	K562	blood
45	chr12:74691800-74692200	Enhancers	K562	blood
46	chr12:74703600-74704000	Enhancers	Fetal Heart	heart
47	chr12:74704400-74704600	Enhancers	Fetal Heart	heart
48	chr12:74709200-74709400	Enhancers	Ovary	ovary
49	chr12:74709800-74711200	Weak transcription	Ovary	ovary
50	chr12:74710200-74711400	Enhancers	Muscle Satellite Cultured Cells	--

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