Variant report

Variant	nsv899134
Chromosome Location	chr12:60141518-60263723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:60174486-60174690	GM12878	blood:	n/a	n/a
2	CEBPB	chr12:60190660-60190908	IMR90	lung:	n/a	chr12:60190769-60190780
3	CEBPB	chr12:60214574-60214865	A549	lung:	n/a	chr12:60214730-60214741
4	CEBPB	chr12:60190709-60190882	A549	lung:	n/a	chr12:60190769-60190780
5	CEBPB	chr12:60167068-60167230	HepG2	liver:	n/a	chr12:60167176-60167187
6	CEBPB	chr12:60190635-60190912	HepG2	liver:	n/a	chr12:60190769-60190780
7	CEBPB	chr12:60214628-60214847	Hela-S3	cervix:	n/a	chr12:60214730-60214741
8	CEBPB	chr12:60214615-60214860	HepG2	liver:	n/a	chr12:60214730-60214741
9	CEBPB	chr12:60190587-60190853	MCF-7	breast:	n/a	chr12:60190769-60190780
10	CEBPB	chr12:60246162-60246440	HepG2	liver:	n/a	chr12:60246256-60246265 chr12:60246254-60246267
11	CEBPB	chr12:60202229-60202494	MCF-7	breast:	n/a	n/a
12	CEBPB	chr12:60218649-60218854	HepG2	liver:	n/a	chr12:60218812-60218823
13	CEBPB	chr12:60193571-60193636	A549	lung:	n/a	n/a
14	CEBPB	chr12:60214552-60214941	IMR90	lung:	n/a	chr12:60214730-60214741
15	CHD2	chr12:60190427-60190459	GM12878	blood:	n/a	n/a
16	CTCF	chr12:60202820-60202970	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr12:60174640-60174790	HMF	breast:	n/a	n/a
18	CTCF	chr12:60174620-60174770	GM12873	blood:	n/a	n/a
19	CTCF	chr12:60202160-60202310	NHDF-neo	bronchial:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
20	CTCF	chr12:60174640-60174790	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr12:60202240-60202390	GM12868	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
22	CTCF	chr12:60174700-60174850	AG04450	lung:	n/a	n/a
23	CTCF	chr12:60174600-60174750	GM12871	blood:	n/a	n/a
24	CTCF	chr12:60228840-60228990	BE2_C	brain:	n/a	n/a
25	CTCF	chr12:60228960-60229110	A549	lung:	n/a	n/a
26	CTCF	chr12:60202240-60202390	HepG2	liver:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
27	CTCF	chr12:60229180-60229330	Caco-2	colon:	n/a	n/a
28	CTCF	chr12:60202198-60202401	Kidney_OC	kidney:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
29	CTCF	chr12:60174640-60174790	NB4	blood:	n/a	n/a
30	CTCF	chr12:60202160-60202310	GM12864	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
31	CTCF	chr12:60202220-60202370	AG10803	skin:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
32	CTCF	chr12:60202180-60202330	WERI-Rb-1	eye:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
33	CTCF	chr12:60174620-60174770	GM12865	blood:	n/a	n/a
34	CTCF	chr12:60228860-60229150	HCM	heart:	n/a	n/a
35	CTCF	chr12:60174620-60174770	HVMF	connective:	n/a	n/a
36	CTCF	chr12:60228880-60229030	GM06990	blood:	n/a	n/a
37	CTCF	chr12:60202220-60202370	GM12864	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
38	CTCF	chr12:60174624-60174788	Medullo	brain:	n/a	n/a
39	CTCF	chr12:60174640-60174790	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr12:60262600-60262750	AG09319	gingival:	n/a	n/a
41	CTCF	chr12:60174675-60174791	GM13977	blood:	n/a	n/a
42	CTCF	chr12:60202220-60202370	BE2_C	brain:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
43	CTCF	chr12:60174660-60174810	GM12872	blood:	n/a	n/a
44	CTCF	chr12:60202900-60203050	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr12:60174700-60174850	BJ	skin:	n/a	n/a
46	CTCF	chr12:60174640-60174824	GM12878	blood:	n/a	n/a
47	CTCF	chr12:60202240-60202390	HEEpiC	esophagus:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
48	CTCF	chr12:60202140-60202290	WI-38	lung:	n/a	n/a
49	CTCF	chr12:60228860-60229010	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr12:60228860-60229010	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60145067-60145117	T-47D	breast:	n/a
2	chr12:60145067-60145117	ovcar-3	ovarian:	n/a
3	chr12:60174815-60174865	AG10803	skin:	n/a
4	chr12:60145067-60145117	AG04449	skin:	fetal
5	chr12:60174815-60174865	MCF-7	breast:	n/a
6	chr12:60145067-60145117	HL-60	blood:	n/a
7	chr12:60174815-60174865	ovcar-3	ovarian:	n/a
8	chr12:60174815-60174865	AG04450	lung:	fetal
9	chr12:60145067-60145117	GM19239	blood:	n/a
10	chr12:60145067-60145117	HCPEpiC	choroid plexus:	n/a
11	chr12:60145067-60145117	HMEC	breast:	n/a
12	chr12:60145067-60145117	A549	lung:	n/a
13	chr12:60145067-60145117	PANC-1	pancreas:	n/a
14	chr12:60174815-60174865	T-47D	breast:	n/a
15	chr12:60174815-60174865	HCF	heart:	n/a
16	chr12:60174815-60174865	ECC-1	luminal epithelium:	n/a
17	chr12:60174815-60174865	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:60145067-60145117	HUVEC	blood vessel:	n/a
19	chr12:60174815-60174865	NH-A	brain:	n/a
20	chr12:60174815-60174865	AG09309	skin:	n/a
21	chr12:60174815-60174865	HMEC	breast:	n/a
22	chr12:60145067-60145117	CMK	blood:	n/a
23	chr12:60174815-60174865	NT2-D1	testis:	n/a
24	chr12:60174815-60174865	GM06990	blood:	n/a
25	chr12:60145067-60145117	BJ	skin:	n/a
26	chr12:60145067-60145117	HCT-116	colon:	n/a
27	chr12:60145067-60145117	HEEpiC	esophagus:	n/a
28	chr12:60174815-60174865	SK-N-MC	brain:	n/a
29	chr12:60145067-60145117	GM12891	blood:	n/a
30	chr12:60145067-60145117	GM06990	blood:	n/a
31	chr12:60174815-60174865	HIPEpiC	eye:	n/a
32	chr12:60174815-60174865	SK-N-SH_RA	brain:	n/a
33	chr12:60174815-60174865	RPTEC	kidney:	n/a
34	chr12:60145067-60145117	AG09309	skin:	n/a
35	chr12:60174815-60174865	SAEC	small airway:	n/a
36	chr12:60174815-60174865	PFSK-1	brain:	n/a
37	chr12:60174815-60174865	BE2_C	brain:	n/a
38	chr12:60174815-60174865	Hepatocyte	liver:	n/a
39	chr12:60145067-60145117	AG09319	gingival:	n/a
40	chr12:60145067-60145117	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:60174815-60174865	HNPCEpiC	eye:	n/a
42	chr12:60145067-60145117	NHDF-neo	bronchial:	n/a
43	chr12:60174815-60174865	LNCaP	prostate:	n/a
44	chr12:60174815-60174865	HRE	kidney:	n/a
45	chr12:60174815-60174865	SKMC	muscle:	n/a
46	chr12:60145067-60145117	HRPEpiC	eye:	n/a
47	chr12:60145067-60145117	HepG2	liver:	n/a
48	chr12:60145067-60145117	MCF10A-Er-Src	breast:	n/a
49	chr12:60174815-60174865	BJ	skin:	n/a
50	chr12:60145067-60145117	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:60238154..60241096-chr12:60242921..60244955,3	MCF-7	breast:
2	chr12:59796807..59797458-chr12:60228606..60229339,3	MCF-7	breast:
3	chr12:60260720..60262687-chr12:60264890..60266941,2	MCF-7	breast:
4	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
5	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
6	chr12:60239189..60241040-chr12:60244979..60247901,2	K562	blood:
7	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
8	chr12:60239189..60241040-chr12:60244979..60247901,2	K562	blood:
9	chr12:60201872..60202711-chr12:60228771..60229623,3	MCF-7	breast:
10	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
11	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
12	chr12:60240866..60243089-chr12:60312800..60315129,2	MCF-7	breast:
13	chr12:60201872..60202711-chr12:60228771..60229623,3	MCF-7	breast:
14	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
15	chr12:58933985..58934928-chr12:60228473..60229377,2	K562	blood:
16	chr12:60238154..60241096-chr12:60242921..60244955,3	MCF-7	breast:
17	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237176	TF binding region
SLC16A7	TF binding region
ENSG00000237176	CpG island
SLC16A7	CpG island

Extended variants
information (count: 4578 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4578 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369474075	chr12:60141518-60141519	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs557162978	chr12:60141602-60141603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79354343	chr12:60141707-60141708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138948379	chr12:60141719-60141720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539678852	chr12:60141744-60141745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552970285	chr12:60141796-60141797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111839501	chr12:60141830-60141831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538412381	chr12:60141899-60141900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573137891	chr12:60141911-60141912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541850504	chr12:60141940-60141941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76262854	chr12:60141948-60141949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184915758	chr12:60141994-60141995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188178484	chr12:60142025-60142026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564309335	chr12:60142035-60142036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76385438	chr12:60142045-60142046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575207662	chr12:60142046-60142047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537947958	chr12:60142098-60142099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77594811	chr12:60142099-60142100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145748805	chr12:60142159-60142160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114785813	chr12:60142191-60142192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547825382	chr12:60142213-60142214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568067758	chr12:60142215-60142216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537105928	chr12:60142240-60142241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148937184	chr12:60142241-60142242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550679361	chr12:60142242-60142243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113634663	chr12:60142257-60142258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145646074	chr12:60142279-60142280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374396001	chr12:60142283-60142284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77660468	chr12:60142289-60142290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368320801	chr12:60142299-60142300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192933969	chr12:60142316-60142317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146538861	chr12:60142383-60142384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544107214	chr12:60142396-60142397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185117705	chr12:60142446-60142447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57198792	chr12:60142488-60142489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35755432	chr12:60142506-60142507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12307037	chr12:60142522-60142523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540429151	chr12:60142534-60142535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560738975	chr12:60142561-60142562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2711694	chr12:60142575-60142576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs77102172	chr12:60142593-60142594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2711693	chr12:60142597-60142598	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530496539	chr12:60142632-60142633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189476227	chr12:60142693-60142694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550642150	chr12:60142744-60142745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570551020	chr12:60142752-60142753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182077240	chr12:60142768-60142769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559902227	chr12:60142770-60142771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566681968	chr12:60142806-60142807	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs535354095	chr12:60142816-60142817	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60099600-60143200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:60100000-60175200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr12:60113000-60143600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr12:60124000-60168800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr12:60127800-60143000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr12:60127800-60143200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr12:60128200-60143000	Weak transcription	Gastric	stomach
8	chr12:60130800-60142800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:60130800-60172200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:60131000-60186000	Weak transcription	Pancreas	Pancrea
11	chr12:60132400-60165600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr12:60136400-60142800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:60137400-60161000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:60138000-60147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:60138400-60141800	Strong transcription	Primary B cells from cord blood	blood
16	chr12:60138600-60168400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:60138800-60141600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:60138800-60141600	Weak transcription	Right Ventricle	heart
19	chr12:60138800-60142200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr12:60138800-60142800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:60138800-60143200	Weak transcription	Left Ventricle	heart
22	chr12:60138800-60173200	Weak transcription	Aorta	Aorta
23	chr12:60139000-60144600	Weak transcription	Adipose Nuclei	Adipose
24	chr12:60139400-60141800	Weak transcription	GM12878-XiMat	blood
25	chr12:60141200-60141600	ZNF genes & repeats	Primary T cells from cord blood	blood
26	chr12:60141400-60141600	ZNF genes & repeats	Dnd41	blood
27	chr12:60141600-60143000	Weak transcription	Dnd41	blood
28	chr12:60141800-60161000	Weak transcription	Primary B cells from cord blood	blood
29	chr12:60142800-60143400	ZNF genes & repeats	Primary T cells from cord blood	blood
30	chr12:60142800-60143600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:60142800-60143800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
32	chr12:60143000-60143400	ZNF genes & repeats	Dnd41	blood
33	chr12:60143000-60143600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr12:60143200-60143400	Enhancers	Left Ventricle	heart
35	chr12:60143400-60157000	Weak transcription	Primary T cells from cord blood	blood
36	chr12:60151400-60152000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:60152000-60182200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr12:60154000-60154800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:60154000-60154800	Enhancers	Fetal Heart	heart
40	chr12:60154800-60157600	Weak transcription	Fetal Heart	heart
41	chr12:60157000-60157400	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr12:60157400-60158000	Strong transcription	Primary T cells from cord blood	blood
43	chr12:60157600-60158000	Enhancers	Fetal Heart	heart
44	chr12:60157600-60158000	ZNF genes & repeats	GM12878-XiMat	blood
45	chr12:60158000-60160800	Weak transcription	GM12878-XiMat	blood
46	chr12:60158000-60161000	Weak transcription	Primary T cells from cord blood	blood
47	chr12:60159000-60168400	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr12:60159000-60172000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr12:60159400-60161000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:60159800-60186400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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