Variant report

Variant	nsv558302
Chromosome Location	chr12:34256210-34342352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:529)
CpG islands
(count:1098)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34276078-34276334	K562	blood:	n/a	n/a
2	ARID3A	chr12:34276092-34276305	HepG2	liver:	n/a	n/a
3	ATF1	chr12:34276078-34276281	K562	blood:	n/a	n/a
4	ATF1	chr12:34280414-34280639	K562	blood:	n/a	n/a
5	ATF1	chr12:34340026-34340130	K562	blood:	n/a	n/a
6	ATF3	chr12:34275984-34276254	GM12878	blood:	n/a	n/a
7	ATF3	chr12:34280320-34280675	K562	blood:	n/a	n/a
8	BATF	chr12:34279173-34279432	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:34276036-34276284	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:34275971-34276281	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:34328719-34328742	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:34280564-34280568	K562	blood:	n/a	n/a
13	BHLHE40	chr12:34276076-34276276	K562	blood:	n/a	n/a
14	BHLHE40	chr12:34279407-34279583	K562	blood:	n/a	n/a
15	BRCA1	chr12:34276078-34276312	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr12:34295564-34295571	GM12878	blood:	n/a	n/a
17	CBX3	chr12:34280337-34280711	K562	blood:	n/a	n/a
18	CBX3	chr12:34286464-34286764	K562	blood:	n/a	n/a
19	CBX3	chr12:34280367-34280675	K562	blood:	n/a	n/a
20	CBX3	chr12:34286882-34287265	K562	blood:	n/a	n/a
21	CEBPB	chr12:34276065-34276346	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:34276061-34276351	K562	blood:	n/a	n/a
23	CEBPB	chr12:34341968-34342276	HepG2	liver:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
24	CEBPB	chr12:34270808-34271042	K562	blood:	n/a	n/a
25	CEBPB	chr12:34280269-34280635	K562	blood:	n/a	n/a
26	CEBPB	chr12:34341921-34342286	K562	blood:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
27	CEBPB	chr12:34276002-34276280	K562	blood:	n/a	n/a
28	CEBPB	chr12:34276033-34276379	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:34280240-34280617	K562	blood:	n/a	n/a
30	CEBPB	chr12:34342050-34342161	H1-hESC	embryonic stem cell:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
31	CEBPB	chr12:34341977-34342278	A549	lung:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
32	CEBPB	chr12:34276029-34276357	IMR90	lung:	n/a	n/a
33	CEBPB	chr12:34306824-34306969	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:34276086-34276337	A549	lung:	n/a	n/a
35	CEBPB	chr12:34341921-34342283	IMR90	lung:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
36	CEBPD	chr12:34280297-34280803	K562	blood:	n/a	n/a
37	CHD2	chr12:34279189-34279391	GM12878	blood:	n/a	n/a
38	CTCF	chr12:34275660-34275810	GM12864	blood:	n/a	n/a
39	CTCF	chr12:34276080-34276230	GM12867	blood:	n/a	n/a
40	CTCF	chr12:34276529-34276616	Gliobla	brain:	n/a	n/a
41	CTCF	chr12:34276040-34276190	GM12864	blood:	n/a	n/a
42	CTCF	chr12:34276019-34276361	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:34276026-34276364	GM19240	blood:	n/a	n/a
44	CTCF	chr12:34276057-34276311	GM19239	blood:	n/a	n/a
45	CTCF	chr12:34276120-34276270	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:34268712-34268761	LNCaP	prostate:	n/a	n/a
47	CTCF	chr12:34275951-34276023	GM12892	blood:	n/a	n/a
48	CTCF	chr12:34323980-34324130	AG09309	skin:	n/a	n/a
49	CTCF	chr12:34286920-34287070	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:34275903-34276423	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34318527-34318577	SKMC	muscle:	n/a
2	chr12:34319734-34319784	AG04449	skin:	fetal
3	chr12:34319822-34319872	T-47D	breast:	n/a
4	chr12:34261436-34261486	AG09319	gingival:	n/a
5	chr12:34260737-34260787	NB4	blood:	n/a
6	chr12:34318115-34318165	SAEC	small airway:	n/a
7	chr12:34318704-34318754	SK-N-SH_RA	brain:	n/a
8	chr12:34259098-34259148	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:34317569-34317619	AoSMC	blood vessel:	n/a
10	chr12:34319740-34319790	GM12892	blood:	n/a
11	chr12:34320121-34320171	AG04449	skin:	fetal
12	chr12:34259098-34259148	NH-A	brain:	n/a
13	chr12:34317983-34318033	HCPEpiC	choroid plexus:	n/a
14	chr12:34319939-34319989	NB4	blood:	n/a
15	chr12:34319740-34319790	T-47D	breast:	n/a
16	chr12:34317983-34318033	NHBE	bronchial:	n/a
17	chr12:34318527-34318577	SK-N-SH_RA	brain:	n/a
18	chr12:34261006-34261056	CMK	blood:	n/a
19	chr12:34318115-34318165	Jurkat	blood:	n/a
20	chr12:34319734-34319784	Hela-S3	cervix:	n/a
21	chr12:34259098-34259148	HCPEpiC	choroid plexus:	n/a
22	chr12:34318704-34318754	NHDF-neo	bronchial:	n/a
23	chr12:34317569-34317619	HepG2	liver:	n/a
24	chr12:34261006-34261056	HRE	kidney:	n/a
25	chr12:34319822-34319872	SKMC	muscle:	n/a
26	chr12:34262100-34262150	K562	blood:	n/a
27	chr12:34318115-34318165	K562	blood:	n/a
28	chr12:34319734-34319784	NHBE	bronchial:	n/a
29	chr12:34317983-34318033	GM06990	blood:	n/a
30	chr12:34319939-34319989	ovcar-3	ovarian:	n/a
31	chr12:34323943-34323993	HEK293	kidney:	embryo
32	chr12:34261006-34261056	NHDF-neo	bronchial:	n/a
33	chr12:34318704-34318754	HEEpiC	esophagus:	n/a
34	chr12:34320121-34320171	HUVEC	blood vessel:	n/a
35	chr12:34323943-34323993	SAEC	small airway:	n/a
36	chr12:34318527-34318577	HUVEC	blood vessel:	n/a
37	chr12:34320121-34320171	HMEC	breast:	n/a
38	chr12:34261116-34261166	HL-60	blood:	n/a
39	chr12:34319740-34319790	BE2_C	brain:	n/a
40	chr12:34319822-34319872	HMEC	breast:	n/a
41	chr12:34318115-34318165	HEK293	kidney:	embryo
42	chr12:34319822-34319872	AG04450	lung:	fetal
43	chr12:34260737-34260787	NHBE	bronchial:	n/a
44	chr12:34261006-34261056	PANC-1	pancreas:	n/a
45	chr12:34260737-34260787	HCF	heart:	n/a
46	chr12:34261006-34261056	MCF10A-Er-Src	breast:	n/a
47	chr12:34261006-34261056	ProgFib	skin:	n/a
48	chr12:34261436-34261486	PrEC	prostate:	n/a
49	chr12:34260737-34260787	HAEpiC	amniotic membrane:	n/a
50	chr12:34319734-34319784	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
2	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
3	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
4	chr12:34275135..34276661-chr12:34371105..34372093,8	K562	blood:
5	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
6	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
7	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
8	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
9	chr1:227730297..227731134-chr12:34260025..34260625,2	MCF-7	breast:
10	chr12:34275660..34276572-chr12:34778082..34778680,2	MCF-7	breast:
11	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
12	chr12:34275751..34276656-chr12:34370666..34371823,3	MCF-7	breast:
13	chr12:34276079..34276686-chr12:34371078..34371813,4	MCF-7	breast:
14	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
15	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-2	chr12:34315112-34315173	ENSG00000255628
2	lnc-ALG10-2	chr12:34309116-34309255	ENSG00000255628
3	lnc-ALG10-2	chr12:34302774-34303105	ENSG00000255628
4	lnc-ALG10-3	chr12:34315397-34315903	NONHSAT027653

No data

Variant related genes	Relation type
ENSG00000256986	TF binding region
TUBB8P4	TF binding region
ENSG00000255628	TF binding region
ENSG00000256986	CpG island
TUBB8P4	CpG island
ENSG00000255628	CpG island
ENSG00000255652	chromatin interactions

Extended variants
information (count: 1813 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1813 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547184990	chr12:34258467-34258468	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs563138471	chr12:34258472-34258473	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs189650813	chr12:34258517-34258518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs552003308	chr12:34258555-34258556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs11053124	chr12:34258556-34258557	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs138899810	chr12:34258557-34258558	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs56660926	chr12:34258579-34258580	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536616141	chr12:34258593-34258594	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs555251785	chr12:34258617-34258618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs575149392	chr12:34258618-34258619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs117445376	chr12:34258645-34258646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs181117452	chr12:34258703-34258704	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs577700478	chr12:34258719-34258720	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs147115519	chr12:34258735-34258736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs376764141	chr12:34258747-34258748	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs186607431	chr12:34258781-34258782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs188938219	chr12:34258893-34258894	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs181670065	chr12:34258923-34258924	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs113327371	chr12:34258924-34258925	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs563225474	chr12:34258946-34258947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs10772145	chr12:34258948-34258949	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545654267	chr12:34258968-34258969	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs186208080	chr12:34258995-34258996	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs527858606	chr12:34259004-34259005	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs547591340	chr12:34259024-34259025	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs149492443	chr12:34259067-34259068	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs567712115	chr12:34259098-34259099	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs113420338	chr12:34259099-34259100	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs549761339	chr12:34259117-34259118	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs568852482	chr12:34259119-34259120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs78101791	chr12:34259151-34259152	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs28477706	chr12:34259191-34259192	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571371784	chr12:34259203-34259204	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs552446585	chr12:34259212-34259213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs143880074	chr12:34259219-34259220	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs573631411	chr12:34259236-34259237	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs542688019	chr12:34259244-34259245	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs556182229	chr12:34259256-34259257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs576838616	chr12:34259303-34259304	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs545740230	chr12:34259393-34259394	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs144232716	chr12:34259441-34259442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs576277457	chr12:34259478-34259479	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs527891037	chr12:34259483-34259484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs569317136	chr12:34259489-34259490	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs148332459	chr12:34259566-34259567	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs561271819	chr12:34259574-34259575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs543358182	chr12:34259579-34259580	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs530123356	chr12:34259597-34259598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs141460749	chr12:34259607-34259608	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs549796786	chr12:34259648-34259649	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34258400-34263200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:34258600-34262800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:34259600-34259800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:34259800-34260200	Bivalent/Poised TSS	Right Ventricle	heart
5	chr12:34259800-34262800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:34260000-34260200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
7	chr12:34260000-34260200	Bivalent Enhancer	Lung	lung
8	chr12:34260000-34261000	Enhancers	Pancreas	Pancrea
9	chr12:34260400-34260800	Bivalent Enhancer	Liver	Liver
10	chr12:34260600-34260800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:34260600-34260800	Bivalent Enhancer	Adipose Nuclei	Adipose
12	chr12:34260600-34260800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
13	chr12:34260600-34262000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:34260800-34261000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:34260800-34261000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:34260800-34261000	Bivalent Enhancer	Lung	lung
17	chr12:34260800-34261000	Bivalent/Poised TSS	Ovary	ovary
18	chr12:34260800-34261200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
19	chr12:34260800-34261200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:34260800-34261200	Enhancers	Liver	Liver
21	chr12:34260800-34261200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
22	chr12:34260800-34261400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr12:34260800-34261400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
24	chr12:34261000-34261200	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:34261000-34261200	Flanking Bivalent TSS/Enh	Ovary	ovary
26	chr12:34261000-34261400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:34261000-34261400	Flanking Active TSS	Pancreas	Pancrea
28	chr12:34261000-34261400	Active TSS	Right Atrium	heart
29	chr12:34261200-34261400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
30	chr12:34261200-34261400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:34261200-34261400	Bivalent Enhancer	Right Ventricle	heart
32	chr12:34261200-34261400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
33	chr12:34261200-34264600	Enhancers	Placenta	Placenta
34	chr12:34261400-34261800	Bivalent Enhancer	Adipose Nuclei	Adipose
35	chr12:34261400-34263000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:34261400-34263600	Weak transcription	Right Atrium	heart
37	chr12:34263000-34264400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:34271200-34271600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:34272200-34272800	Enhancers	Adipose Nuclei	Adipose
40	chr12:34272800-34275200	Weak transcription	Adipose Nuclei	Adipose
41	chr12:34274200-34274600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:34274200-34275200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
43	chr12:34275000-34275800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:34275200-34275800	Enhancers	Adipose Nuclei	Adipose
45	chr12:34275200-34275800	Enhancers	Placenta	Placenta
46	chr12:34275800-34276200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr12:34275800-34278600	Weak transcription	Adipose Nuclei	Adipose
48	chr12:34275800-34278600	Weak transcription	Placenta	Placenta
49	chr12:34276600-34276800	Enhancers	Lung	lung
50	chr12:34276600-34276800	Enhancers	K562	blood

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