Variant report

Variant	esv3382230
Chromosome Location	chr12:11205667-11249323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
2	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
3	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
4	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
5	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
6	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
7	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
8	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
9	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
10	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
14	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
18	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
19	CTCF	chr12:11206452-11206523	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
22	CTCF	chr12:11209820-11209970	HEK293	kidney:	n/a	n/a
23	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
24	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
25	CTCF	chr12:11209700-11209850	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:11209740-11209890	HepG2	liver:	n/a	n/a
27	CTCF	chr12:11209872-11209908	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:11207523-11207552	GM10248	blood:	n/a	n/a
29	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
30	E2F4	chr12:11205619-11205672	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
33	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
34	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
35	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
36	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
37	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
38	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
39	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
40	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
41	FOXA2	chr12:11223617-11224724	HepG2	liver:	n/a	n/a
42	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
43	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a
44	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a
45	GATA3	chr12:11221936-11222225	MCF-7	breast:	n/a	n/a
46	HDAC2	chr12:11223990-11224345	HepG2	liver:	n/a	n/a
47	IKZF1	chr12:11238336-11238561	GM12878	blood:	n/a	n/a
48	IRF1	chr12:11208646-11208659	K562	blood:	n/a	n/a
49	IRF4	chr12:11247559-11247865	GM12878	blood:	n/a	n/a
50	IRF4	chr12:11247411-11247911	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244939-11244989	AG10803	skin:	n/a
2	chr12:11244899-11244949	SAEC	small airway:	n/a
3	chr12:11215083-11215133	AoSMC	blood vessel:	n/a
4	chr12:11215083-11215133	SK-N-SH	brain:	n/a
5	chr12:11216351-11216401	AG09319	gingival:	n/a
6	chr12:11244939-11244989	HepG2	liver:	n/a
7	chr12:11244899-11244949	SK-N-SH_RA	brain:	n/a
8	chr12:11244939-11244989	NHDF-neo	bronchial:	n/a
9	chr12:11244939-11244989	HCM	heart:	n/a
10	chr12:11244899-11244949	GM19239	blood:	n/a
11	chr12:11244899-11244949	IMR90	lung:	fetal
12	chr12:11216351-11216401	HRPEpiC	eye:	n/a
13	chr12:11244899-11244949	GM06990	blood:	n/a
14	chr12:11215083-11215133	MCF10A-Er-Src	breast:	n/a
15	chr12:11244939-11244989	HMEC	breast:	n/a
16	chr12:11244939-11244989	H1-hESC	embryonic stem cell:	embryo
17	chr12:11244899-11244949	HAEpiC	amniotic membrane:	n/a
18	chr12:11216351-11216401	HCPEpiC	choroid plexus:	n/a
19	chr12:11216351-11216401	CMK	blood:	n/a
20	chr12:11244899-11244949	HEK293	kidney:	embryo
21	chr12:11244939-11244989	HUVEC	blood vessel:	n/a
22	chr12:11244939-11244989	T-47D	breast:	n/a
23	chr12:11244899-11244949	NHBE	bronchial:	n/a
24	chr12:11216351-11216401	HRE	kidney:	n/a
25	chr12:11215083-11215133	AG04450	lung:	fetal
26	chr12:11216351-11216401	GM12878	blood:	n/a
27	chr12:11215083-11215133	ProgFib	skin:	n/a
28	chr12:11216351-11216401	MCF10A-Er-Src	breast:	n/a
29	chr12:11215083-11215133	HNPCEpiC	eye:	n/a
30	chr12:11216351-11216401	AG04450	lung:	fetal
31	chr12:11215083-11215133	A549	lung:	n/a
32	chr12:11244899-11244949	MCF10A-Er-Src	breast:	n/a
33	chr12:11244899-11244949	A549	lung:	n/a
34	chr12:11215083-11215133	U87	brain:	n/a
35	chr12:11215083-11215133	HCPEpiC	choroid plexus:	n/a
36	chr12:11244899-11244949	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:11216351-11216401	HRCEpiC	kidney:	n/a
38	chr12:11215083-11215133	GM12892	blood:	n/a
39	chr12:11215083-11215133	AG09309	skin:	n/a
40	chr12:11244939-11244989	HCF	heart:	n/a
41	chr12:11216351-11216401	HUVEC	blood vessel:	n/a
42	chr12:11215083-11215133	ECC-1	luminal epithelium:	n/a
43	chr12:11215083-11215133	HEK293	kidney:	embryo
44	chr12:11215083-11215133	HRCEpiC	kidney:	n/a
45	chr12:11244939-11244989	SAEC	small airway:	n/a
46	chr12:11244899-11244949	SK-N-MC	brain:	n/a
47	chr12:11215083-11215133	AG04449	skin:	fetal
48	chr12:11215083-11215133	PANC-1	pancreas:	n/a
49	chr12:11216351-11216401	AG04449	skin:	fetal
50	chr12:11244899-11244949	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
2	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056
2	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R63P	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
TAS2R63P	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 2699 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2699 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4763236	chr12:11205673-11205674	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78279906	chr12:11205674-11205675	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112848831	chr12:11205675-11205676	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74681880	chr12:11205676-11205677	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374622363	chr12:11205683-11205684	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77925716	chr12:11205710-11205711	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78030941	chr12:11205726-11205727	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200684188	chr12:11205728-11205729	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141718945	chr12:11205750-11205751	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74496068	chr12:11205756-11205757	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78087450	chr12:11205769-11205770	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2256739	chr12:11205798-11205799	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs2708387	chr12:11205904-11205905	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs201407644	chr12:11205926-11205927	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs541700299	chr12:11205931-11205932	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs74734008	chr12:11205938-11205939	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs367963949	chr12:11205965-11205966	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs549519163	chr12:11205986-11205987	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs142320892	chr12:11206035-11206036	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs113748752	chr12:11206066-11206067	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs561368349	chr12:11206070-11206071	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs79863703	chr12:11206074-11206075	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs80330801	chr12:11206098-11206099	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs79539381	chr12:11206202-11206203	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs188756395	chr12:11206212-11206213	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs2597994	chr12:11206217-11206218	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs563413715	chr12:11206221-11206222	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376590252	chr12:11206247-11206248	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs371111255	chr12:11206261-11206262	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs72477404	chr12:11206279-11206280	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369700821	chr12:11206313-11206314	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs532375104	chr12:11206346-11206347	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370683243	chr12:11206363-11206364	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs375351551	chr12:11206367-11206368	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200049613	chr12:11206380-11206381	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191455802	chr12:11206449-11206450	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183310846	chr12:11206450-11206451	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs528424835	chr12:11206455-11206456	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs145063228	chr12:11206505-11206506	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs568199657	chr12:11206521-11206522	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534009385	chr12:11206545-11206546	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs537218386	chr12:11206603-11206604	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs554008976	chr12:11206719-11206720	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs529489876	chr12:11206753-11206754	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs79497235	chr12:11206765-11206766	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs532406974	chr12:11206782-11206783	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs550713495	chr12:11206812-11206813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61912889	chr12:11206816-11206817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144929457	chr12:11206828-11206829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553042601	chr12:11206850-11206851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:11168800-11205800	Weak transcription	Osteobl	bone
3	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel
4	chr12:11171000-11225600	Weak transcription	HSMMtube	muscle
5	chr12:11176400-11211200	Weak transcription	Aorta	Aorta
6	chr12:11179000-11223800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr12:11179400-11222000	Weak transcription	Fetal Kidney	kidney
8	chr12:11181000-11217400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:11181000-11220000	Weak transcription	Gastric	stomach
10	chr12:11181000-11224800	Weak transcription	Fetal Stomach	stomach
11	chr12:11181600-11209400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr12:11184200-11213000	Weak transcription	Thymus	Thymus
13	chr12:11193200-11224200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:11194600-11210000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr12:11196600-11211400	Weak transcription	Fetal Heart	heart
16	chr12:11196600-11215000	Weak transcription	NHLF	lung
17	chr12:11198000-11230200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr12:11199600-11214200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:11199800-11206200	Weak transcription	Fetal Intestine Large	intestine
20	chr12:11199800-11222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:11201000-11206800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:11201400-11210600	Weak transcription	Left Ventricle	heart
23	chr12:11201600-11227800	Weak transcription	HSMM	muscle
24	chr12:11203000-11205800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:11203200-11206400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr12:11203200-11211600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:11203600-11206400	Weak transcription	Fetal Brain Male	brain
28	chr12:11203600-11209400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:11203600-11216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:11203600-11240000	Weak transcription	Ovary	ovary
31	chr12:11203800-11207800	Weak transcription	A549	lung
32	chr12:11203800-11211200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr12:11203800-11211400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:11203800-11211600	Weak transcription	Hela-S3	cervix
35	chr12:11203800-11212200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr12:11203800-11212400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:11204400-11209200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr12:11204600-11224000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:11204600-11227600	Weak transcription	Fetal Lung	lung
41	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr12:11205000-11205800	ZNF genes & repeats	Primary B cells from cord blood	blood
43	chr12:11205800-11218200	Weak transcription	Primary B cells from cord blood	blood
44	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:11206000-11221600	Weak transcription	Fetal Muscle Leg	muscle
46	chr12:11206400-11207800	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr12:11206800-11207800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:11207000-11209000	Weak transcription	Primary hematopoietic stem cells	blood
49	chr12:11207000-11223000	Weak transcription	HepG2	liver
50	chr12:11207000-11224200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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