Variant report

Variant	nsv518946
Chromosome Location	chr12:854331-961336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2945)
CpG islands
(count:915)
Chromatin interactive
region (count:107)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2945 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:899820-900011	K562	blood:	n/a	n/a
2	ARID3A	chr12:925667-926004	K562	blood:	n/a	n/a
3	ARID3A	chr12:860968-861705	HepG2	liver:	n/a	chr12:861103-861119
4	ARID3A	chr12:923375-923763	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:859850-860665	K562	blood:	n/a	n/a
6	ARID3A	chr12:925672-925952	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:904508-904691	K562	blood:	n/a	n/a
8	ARID3A	chr12:860435-860729	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:861036-861605	K562	blood:	n/a	chr12:861103-861119
10	ARID3A	chr12:888927-889307	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:864137-864680	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:886012-886221	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:863980-864603	K562	blood:	n/a	n/a
14	ARID3A	chr12:923400-923725	K562	blood:	n/a	n/a
15	ARID3A	chr12:914118-914158	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:899446-899520	K562	blood:	n/a	n/a
17	ATF1	chr12:861326-861689	K562	blood:	n/a	n/a
18	ATF1	chr12:864177-864588	K562	blood:	n/a	n/a
19	ATF2	chr12:861296-861837	GM12878	blood:	n/a	n/a
20	ATF2	chr12:860111-860867	GM12878	blood:	n/a	n/a
21	ATF2	chr12:919616-920278	GM12878	blood:	n/a	n/a
22	ATF2	chr12:860317-860903	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr12:916459-916858	GM12878	blood:	n/a	n/a
24	ATF2	chr12:916414-916900	GM12878	blood:	n/a	n/a
25	ATF2	chr12:932098-932901	GM12878	blood:	n/a	n/a
26	ATF2	chr12:860283-860868	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr12:860099-860870	GM12878	blood:	n/a	n/a
28	ATF2	chr12:932136-932907	GM12878	blood:	n/a	n/a
29	ATF2	chr12:919620-920364	GM12878	blood:	n/a	n/a
30	ATF3	chr12:860183-860817	A549	lung:	n/a	n/a
31	ATF3	chr12:861345-861689	GM12878	blood:	n/a	n/a
32	ATF3	chr12:861395-861668	K562	blood:	n/a	n/a
33	ATF3	chr12:861305-861867	A549	lung:	n/a	n/a
34	ATF3	chr12:860217-860784	A549	lung:	n/a	n/a
35	ATF3	chr12:861424-861712	HepG2	liver:	n/a	n/a
36	BACH1	chr12:927893-928274	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr12:860059-860703	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr12:922636-922643	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr12:927295-927341	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr12:864141-864402	K562	blood:	n/a	n/a
41	BATF	chr12:919770-920232	GM12878	blood:	n/a	n/a
42	BATF	chr12:919759-920261	GM12878	blood:	n/a	n/a
43	BATF	chr12:860308-860675	GM12878	blood:	n/a	n/a
44	BATF	chr12:888884-889145	GM12878	blood:	n/a	chr12:889023-889034
45	BATF	chr12:898909-899396	GM12878	blood:	n/a	chr12:899377-899386
46	BATF	chr12:888854-889213	GM12878	blood:	n/a	chr12:889023-889034
47	BATF	chr12:901667-901904	GM12878	blood:	n/a	chr12:901756-901767
48	BCL11A	chr12:916571-916782	GM12878	blood:	n/a	chr12:916732-916741
49	BCL11A	chr12:860218-860701	GM12878	blood:	n/a	chr12:860448-860461
50	BCL11A	chr12:919798-920244	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:863472-863522	SK-N-SH_RA	brain:	n/a
2	chr12:886615-886665	ProgFib	skin:	n/a
3	chr12:863605-863655	Caco-2	colon:	n/a
4	chr12:861752-861802	HRE	kidney:	n/a
5	chr12:860787-860837	SK-N-SH	brain:	n/a
6	chr12:861787-861837	GM12892	blood:	n/a
7	chr12:860480-860530	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:860480-860530	PANC-1	pancreas:	n/a
9	chr12:862975-863025	HNPCEpiC	eye:	n/a
10	chr12:886615-886665	SKMC	muscle:	n/a
11	chr12:861469-861519	NT2-D1	testis:	n/a
12	chr12:862663-862713	MCF-7	breast:	n/a
13	chr12:862975-863025	LNCaP	prostate:	n/a
14	chr12:858759-858809	HepG2	liver:	n/a
15	chr12:860520-860570	AG10803	skin:	n/a
16	chr12:863472-863522	NT2-D1	testis:	n/a
17	chr12:860787-860837	HCT-116	colon:	n/a
18	chr12:858759-858809	BE2_C	brain:	n/a
19	chr12:861787-861837	ECC-1	luminal epithelium:	n/a
20	chr12:860520-860570	MCF10A-Er-Src	breast:	n/a
21	chr12:861787-861837	NT2-D1	testis:	n/a
22	chr12:866289-866339	NHDF-neo	bronchial:	n/a
23	chr12:861752-861802	HCPEpiC	choroid plexus:	n/a
24	chr12:861469-861519	Hela-S3	cervix:	n/a
25	chr12:862663-862713	HNPCEpiC	eye:	n/a
26	chr12:862793-862843	SK-N-SH_RA	brain:	n/a
27	chr12:861715-861765	HCT-116	colon:	n/a
28	chr12:863472-863522	HRPEpiC	eye:	n/a
29	chr12:862975-863025	ECC-1	luminal epithelium:	n/a
30	chr12:858759-858809	SK-N-MC	brain:	n/a
31	chr12:858759-858809	LNCaP	prostate:	n/a
32	chr12:860480-860530	H1-hESC	embryonic stem cell:	embryo
33	chr12:860787-860837	GM12878	blood:	n/a
34	chr12:861752-861802	HIPEpiC	eye:	n/a
35	chr12:861787-861837	SKMC	muscle:	n/a
36	chr12:862975-863025	PFSK-1	brain:	n/a
37	chr12:858759-858809	ECC-1	luminal epithelium:	n/a
38	chr12:862663-862713	AoSMC	blood vessel:	n/a
39	chr12:860787-860837	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:863605-863655	NB4	blood:	n/a
41	chr12:862793-862843	PANC-1	pancreas:	n/a
42	chr12:862975-863025	H1-hESC	embryonic stem cell:	embryo
43	chr12:862663-862713	PFSK-1	brain:	n/a
44	chr12:863472-863522	HepG2	liver:	n/a
45	chr12:886615-886665	Hepatocyte	liver:	n/a
46	chr12:862793-862843	GM12892	blood:	n/a
47	chr12:860787-860837	GM06990	blood:	n/a
48	chr12:862793-862843	HUVEC	blood vessel:	n/a
49	chr12:858759-858809	AG09319	gingival:	n/a
50	chr12:866289-866339	NB4	blood:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:849337..852194-chr12:853558..856397,3	K562	blood:
2	chr12:497519..500271-chr12:922921..925641,2	K562	blood:
3	chr12:864103..866169-chr12:883528..885181,2	K562	blood:
4	chr12:860830..863519-chr17:56735307..56737869,2	MCF-7	breast:
5	chr12:860752..862615-chr12:913879..916697,2	K562	blood:
6	chr12:857339..858842-chr12:859156..860743,2	MCF-7	breast:
7	chr12:881327..884915-chr12:893641..898608,4	K562	blood:
8	chr12:678017..679838-chr12:873854..876600,2	K562	blood:
9	chr12:860770..861524-chr9:131102541..131103389,2	Hela-S3	cervix:
10	chr12:876294..878971-chr12:885168..888118,2	K562	blood:
11	chr12:906517..908148-chr12:911108..913048,2	K562	blood:
12	chr12:723353..724122-chr12:860374..861153,4	MCF-7	breast:
13	chr12:723315..723961-chr12:923260..924029,2	MCF-7	breast:
14	chr12:919866..922717-chr12:940854..943432,2	K562	blood:
15	chr12:925748..927383-chr12:929410..931068,2	K562	blood:
16	chr12:860224..860944-chr7:86849375..86850131,2	Hela-S3	cervix:
17	chr12:824399..827215-chr12:865443..868265,2	K562	blood:
18	chr12:728784..730437-chr12:859052..860825,2	MCF-7	breast:
19	chr12:858790..861699-chr12:870992..873821,2	K562	blood:
20	chr12:876367..879119-chr12:880594..883556,3	K562	blood:
21	chr12:861574..863792-chr12:1057514..1060138,2	K562	blood:
22	chr12:825603..828799-chr12:857363..861650,3	K562	blood:
23	chr12:862748..867412-chr12:867871..873426,6	K562	blood:
24	chr12:860587..863557-chr12:905754..908662,2	MCF-7	breast:
25	chr12:845525..848174-chr12:852039..854517,2	MCF-7	breast:
26	chr12:860489..863381-chr12:877011..880566,3	MCF-7	breast:
27	chr12:858968..861238-chr12:1057237..1058981,2	K562	blood:
28	chr12:876294..878971-chr12:885168..888118,2	K562	blood:
29	chr12:876367..879119-chr12:880594..883556,3	K562	blood:
30	chr12:678673..679595-chr12:860437..861048,2	K562	blood:
31	chr12:864121..866273-chr12:867871..870258,2	K562	blood:
32	chr12:862748..867412-chr12:867871..873426,6	K562	blood:
33	chr12:862374..864096-chr12:909523..912296,2	MCF-7	breast:
34	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
35	chr12:851480..853426-chr12:857104..859711,2	K562	blood:
36	chr12:855985..857857-chr12:859146..862006,3	K562	blood:
37	chr12:562106..562698-chr12:860790..861501,2	MCF-7	breast:
38	chr12:940142..943103-chr12:948785..951381,2	MCF-7	breast:
39	chr12:951982..954213-chr12:955947..958050,2	K562	blood:
40	chr12:925748..927383-chr12:929410..931068,2	K562	blood:
41	chr12:676546..679499-chr12:924463..926278,2	K562	blood:
42	chr12:860770..863546-chr12:920587..924774,4	MCF-7	breast:
43	chr12:858790..861699-chr12:870992..873821,2	K562	blood:
44	chr12:684994..685885-chr12:923018..923598,3	K562	blood:
45	chr12:751953..754697-chr12:859970..862221,2	K562	blood:
46	chr12:919540..922758-chr12:931539..933937,3	K562	blood:
47	chr12:678986..679579-chr12:860176..860988,2	MCF-7	breast:
48	chr12:944261..946824-chr12:949779..951935,3	K562	blood:
49	chr12:861293..862206-chr19:10612896..10613598,2	NB4	blood:
50	chr12:940142..943103-chr12:948785..951381,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ2-3	chr12:890139-890879	predAs_chen_BU787457_1

No data

Variant related genes	Relation type
WNK1	TF binding region
RNU4ATAC16P	TF binding region
WNK1	CpG island
RNU4ATAC16P	CpG island
ENSG00000171840	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000136897	chromatin interactions
ENSG00000136870	chromatin interactions
ENSG00000060237	chromatin interactions
ENSG00000256672	chromatin interactions
ENSG00000167114	chromatin interactions
ENSG00000207972	chromatin interactions
ENSG00000177406	chromatin interactions
ENSG00000148516	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000255825	chromatin interactions
ENSG00000237036	chromatin interactions
ENSG00000073614	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000172164	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000079805	chromatin interactions
ENSG00000272502	chromatin interactions

Extended variants
information (count: 3807 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3807 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7137188	chr12:854331-854332	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190436031	chr12:854343-854344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs55974153	chr12:854353-854354	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs527602310	chr12:854384-854385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556094508	chr12:854450-854451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6489744	chr12:854492-854493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182365956	chr12:854522-854523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185362629	chr12:854538-854539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140293712	chr12:854656-854657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113716408	chr12:854664-854665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542724757	chr12:854665-854666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202048138	chr12:854666-854667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60781065	chr12:854668-854669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200158905	chr12:854670-854671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531325277	chr12:854683-854684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551116122	chr12:854689-854690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190147945	chr12:854710-854711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7313243	chr12:854719-854720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376960197	chr12:854736-854737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551689952	chr12:854740-854741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367983528	chr12:854744-854745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6489745	chr12:854757-854758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs138934243	chr12:854765-854766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548980916	chr12:854788-854789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181301932	chr12:854800-854801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537956755	chr12:854801-854802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556321068	chr12:854805-854806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571393504	chr12:854808-854809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7961371	chr12:854818-854819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185523963	chr12:854880-854881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566924726	chr12:854912-854913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189985522	chr12:854923-854924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542612533	chr12:854933-854934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533783085	chr12:854949-854950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180852117	chr12:854962-854963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558311784	chr12:854977-854978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12578864	chr12:854982-854983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35554781	chr12:854984-854985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576777720	chr12:854996-854997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563080173	chr12:855147-855148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533375532	chr12:855171-855172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184916418	chr12:855184-855185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192094462	chr12:855238-855239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560379731	chr12:855310-855311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146331551	chr12:855326-855327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548919591	chr12:855371-855372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555997488	chr12:855381-855382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567600366	chr12:855382-855383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184032484	chr12:855439-855440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188520138	chr12:855600-855601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4479 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:850800-859000	Weak transcription	Fetal Heart	heart
2	chr12:853200-858400	Weak transcription	Primary T cells from cord blood	blood
3	chr12:853200-858800	Weak transcription	HepG2	liver
4	chr12:853200-859800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr12:853400-858000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:853400-858800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:853400-858800	Weak transcription	A549	lung
8	chr12:853600-854400	Enhancers	GM12878-XiMat	blood
9	chr12:853600-854800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr12:853600-858600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:853600-858800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr12:853600-858800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr12:853600-859000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr12:853800-858800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr12:853800-858800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr12:854000-858600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr12:854000-859000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:854000-859200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr12:854400-858400	Weak transcription	GM12878-XiMat	blood
20	chr12:857400-857600	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:857600-859000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:857800-858000	Enhancers	Brain Angular Gyrus	brain
23	chr12:857800-858000	Enhancers	Brain Hippocampus Middle	brain
24	chr12:858000-858200	Enhancers	Brain Cingulate Gyrus	brain
25	chr12:858000-858600	Weak transcription	Brain Angular Gyrus	brain
26	chr12:858000-858800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:858000-859600	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr12:858200-858800	Weak transcription	Brain Cingulate Gyrus	brain
29	chr12:858200-859200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr12:858200-859200	Enhancers	Brain Substantia Nigra	brain
31	chr12:858200-859600	Enhancers	Brain Anterior Caudate	brain
32	chr12:858400-858800	Active TSS	GM12878-XiMat	blood
33	chr12:858400-859200	Enhancers	Primary T cells from cord blood	blood
34	chr12:858400-859200	Enhancers	Hela-S3	cervix
35	chr12:858400-859800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:858400-859800	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr12:858600-859000	Enhancers	Brain Angular Gyrus	brain
38	chr12:858600-859600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr12:858600-859800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr12:858600-860000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr12:858800-859000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:858800-859000	Enhancers	Brain Cingulate Gyrus	brain
43	chr12:858800-859000	Enhancers	Dnd41	blood
44	chr12:858800-859000	Enhancers	K562	blood
45	chr12:858800-859200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr12:858800-859400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr12:858800-859400	Active TSS	Brain Hippocampus Middle	brain
48	chr12:858800-859400	Flanking Active TSS	A549	lung
49	chr12:858800-859400	Flanking Active TSS	GM12878-XiMat	blood
50	chr12:858800-859600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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