Variant report

Variant	esv2466772
Chromosome Location	chr2:133003677-133011561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:183)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133010732-133010763	K562	blood:	n/a	n/a
2	ATF1	chr2:133009295-133009427	K562	blood:	n/a	n/a
3	BACH1	chr2:133011420-133011447	K562	blood:	n/a	n/a
4	BATF	chr2:133004595-133004910	GM12878	blood:	n/a	n/a
5	BATF	chr2:133004391-133004933	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:133003116-133003948	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:133004602-133004902	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:133004381-133004992	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:133004682-133004922	HepG2	liver:	n/a	n/a
10	BHLHE40	chr2:133010563-133010935	K562	blood:	n/a	n/a
11	BHLHE40	chr2:133011384-133011548	K562	blood:	n/a	n/a
12	BRCA1	chr2:133008327-133008364	HepG2	liver:	n/a	n/a
13	BRCA1	chr2:133011420-133013340	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:133011422-133013353	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr2:133009442-133009479	GM12878	blood:	n/a	n/a
16	CCNT2	chr2:133011242-133013338	K562	blood:	n/a	chr2:133011602-133011611
17	CCNT2	chr2:133010554-133010930	K562	blood:	n/a	chr2:133010575-133010584
18	CEBPB	chr2:133010735-133010764	K562	blood:	n/a	n/a
19	CEBPB	chr2:133005007-133005175	HepG2	liver:	n/a	n/a
20	CHD1	chr2:133009318-133009386	GM12878	blood:	n/a	n/a
21	CHD1	chr2:133011417-133013353	GM12878	blood:	n/a	n/a
22	CHD2	chr2:133011247-133013353	K562	blood:	n/a	n/a
23	CHD2	chr2:133011385-133013351	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr2:133010564-133010935	K562	blood:	n/a	n/a
25	CHD2	chr2:133008513-133008625	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:133009436-133009545	GM10266	blood:	n/a	n/a
27	CTCF	chr2:133008940-133009090	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:133008540-133008690	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:133008540-133008690	GM12865	blood:	n/a	n/a
30	CTCF	chr2:133009478-133009572	GM13976	blood:	n/a	n/a
31	CTCF	chr2:133008440-133008590	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr2:133009489-133009506	GM10248	blood:	n/a	n/a
33	CTCF	chr2:133008480-133008630	HAc	cerebellar:	n/a	n/a
34	CTCF	chr2:133008460-133008610	GM12875	blood:	n/a	n/a
35	CTCF	chr2:133008340-133008490	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr2:133008546-133008696	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr2:133009019-133009074	GM10266	blood:	n/a	n/a
38	CTCF	chr2:133008504-133008799	GM10248	blood:	n/a	n/a
39	CTCF	chr2:133009416-133009459	Medullo	brain:	n/a	n/a
40	CTCF	chr2:133009220-133009370	AG10803	skin:	n/a	n/a
41	CTCF	chr2:133008524-133008625	GM10266	blood:	n/a	n/a
42	CTCF	chr2:133011384-133013354	IMR90	lung:	n/a	n/a
43	CTCF	chr2:133008513-133008547	LNCaP	prostate:	n/a	n/a
44	CTCF	chr2:133009340-133009490	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr2:133008420-133008570	HFF	foreskin:	n/a	n/a
46	CTCF	chr2:133008760-133008910	HPF	lung:	n/a	n/a
47	CTCF	chr2:133009432-133009514	LNCaP	prostate:	n/a	n/a
48	CTCF	chr2:133008994-133009059	GM13976	blood:	n/a	n/a
49	CTCF	chr2:133008320-133008470	Caco-2	colon:	n/a	n/a
50	CTCF	chr2:133009300-133009450	NHDF-neo	bronchial:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133010653-133010703	HEK293	kidney:	embryo
2	chr2:133010653-133010703	K562	blood:	n/a
3	chr2:133010653-133010703	PANC-1	pancreas:	n/a
4	chr2:133009869-133009919	ProgFib	skin:	n/a
5	chr2:133008094-133008144	HRCEpiC	kidney:	n/a
6	chr2:133010653-133010703	ovcar-3	ovarian:	n/a
7	chr2:133008094-133008144	NHBE	bronchial:	n/a
8	chr2:133010653-133010703	HCT-116	colon:	n/a
9	chr2:133009869-133009919	HCM	heart:	n/a
10	chr2:133008094-133008144	CMK	blood:	n/a
11	chr2:133008094-133008144	HRE	kidney:	n/a
12	chr2:133008094-133008144	BJ	skin:	n/a
13	chr2:133010653-133010703	GM12891	blood:	n/a
14	chr2:133010653-133010703	HCM	heart:	n/a
15	chr2:133010653-133010703	GM12878	blood:	n/a
16	chr2:133008094-133008144	Jurkat	blood:	n/a
17	chr2:133008094-133008144	MCF10A-Er-Src	breast:	n/a
18	chr2:133009869-133009919	NHDF-neo	bronchial:	n/a
19	chr2:133010653-133010703	AG04449	skin:	fetal
20	chr2:133010653-133010703	AG04450	lung:	fetal
21	chr2:133008094-133008144	ECC-1	luminal epithelium:	n/a
22	chr2:133008094-133008144	HepG2	liver:	n/a
23	chr2:133008094-133008144	SK-N-MC	brain:	n/a
24	chr2:133010653-133010703	SK-N-SH	brain:	n/a
25	chr2:133009869-133009919	NHBE	bronchial:	n/a
26	chr2:133009869-133009919	HEK293	kidney:	embryo
27	chr2:133008094-133008144	SAEC	small airway:	n/a
28	chr2:133009869-133009919	HEEpiC	esophagus:	n/a
29	chr2:133010653-133010703	HNPCEpiC	eye:	n/a
30	chr2:133009869-133009919	SKMC	muscle:	n/a
31	chr2:133009869-133009919	LNCaP	prostate:	n/a
32	chr2:133009869-133009919	SK-N-MC	brain:	n/a
33	chr2:133010653-133010703	AG09319	gingival:	n/a
34	chr2:133009869-133009919	CMK	blood:	n/a
35	chr2:133009869-133009919	A549	lung:	n/a
36	chr2:133009869-133009919	NH-A	brain:	n/a
37	chr2:133010653-133010703	PrEC	prostate:	n/a
38	chr2:133009869-133009919	AG04450	lung:	fetal
39	chr2:133009869-133009919	MCF-7	breast:	n/a
40	chr2:133010653-133010703	H1-hESC	embryonic stem cell:	embryo
41	chr2:133010653-133010703	SAEC	small airway:	n/a
42	chr2:133010653-133010703	NB4	blood:	n/a
43	chr2:133008094-133008144	RPTEC	kidney:	n/a
44	chr2:133008094-133008144	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:133009869-133009919	ECC-1	luminal epithelium:	n/a
46	chr2:133009869-133009919	H1-hESC	embryonic stem cell:	embryo
47	chr2:133009869-133009919	AoSMC	blood vessel:	n/a
48	chr2:133010653-133010703	Hepatocyte	liver:	n/a
49	chr2:133009869-133009919	HUVEC	blood vessel:	n/a
50	chr2:133009869-133009919	SAEC	small airway:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:91851357..91852890-chr2:133010879..133013835,2	K562	blood:
2	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
3	chr2:133011277..133017359-chr20:26187383..26191986,21	K562	blood:
4	chr17:803107..806087-chr2:133011166..133013833,2	K562	blood:
5	chr12:20702911..20705964-chr2:133010767..133014432,7	K562	blood:
6	chr16:33958834..33966480-chr2:133009904..133018933,30	MCF-7	breast:
7	chr12:20702909..20705960-chr2:133011295..133014432,7	K562	blood:
8	chr2:133010317..133016704-chr21:9824094..9829011,32	MCF-7	breast:
9	chr16:33965176..33965978-chr2:133010227..133011402,4	MCF-7	breast:
10	chr1:91853077..91854647-chr2:133009089..133010727,2	K562	blood:
11	chr16:33961661..33967162-chr2:133010338..133015206,18	K562	blood:
12	chr12:20702922..20705906-chr2:133011248..133013650,3	MCF-7	breast:
13	chr16:33961611..33967347-chr2:133008818..133014443,19	K562	blood:
14	chr16:33959973..33964975-chr2:133010437..133015799,15	MCF-7	breast:
15	chr13:24087086..24087588-chr2:133003343..133003844,2	MCF-7	breast:
16	chr2:133010455..133013497-chrX:108295941..108299311,5	K562	blood:
17	chr2:133009402..133016367-chr21:9824030..9829043,35	MCF-7	breast:
18	chr16:33962831..33965453-chr2:133011419..133013464,21	MCF-7	breast:
19	chr1:91852916..91854571-chr2:133011071..133013655,2	K562	blood:
20	chr2:133010417..133016800-chr21:9824146..9829019,50	K562	blood:
21	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
22	chr16:33962970..33965065-chr2:133011472..133013456,38	MCF-7	breast:
23	chr2:133010417..133015279-chr21:9824040..9829010,45	K562	blood:

No data

Variant related genes	Relation type
RNA5-8SP5	TF binding region
RNA5-8SP5	CpG island
ENSG00000264462	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000256642	chromatin interactions

Extended variants
information (count: 1286 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201498955	chr2:133003677-133003678	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199805900	chr2:133003682-133003683	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200237821	chr2:133003704-133003705	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534834956	chr2:133003711-133003712	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377139299	chr2:133003715-133003716	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201371086	chr2:133003730-133003731	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372984106	chr2:133003742-133003743	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376623726	chr2:133003746-133003747	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369022645	chr2:133003748-133003749	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372980046	chr2:133003750-133003751	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375328775	chr2:133003751-133003752	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546639781	chr2:133003761-133003762	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369321251	chr2:133003764-133003765	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199686214	chr2:133003771-133003772	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376321347	chr2:133003774-133003775	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200820673	chr2:133003779-133003780	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201833396	chr2:133003780-133003781	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370604531	chr2:133003785-133003786	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373449867	chr2:133003787-133003788	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145479341	chr2:133003798-133003799	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377437640	chr2:133003799-133003800	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370265548	chr2:133003803-133003804	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568449556	chr2:133003809-133003810	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62164043	chr2:133003813-133003814	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374429618	chr2:133003816-133003817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114794391	chr2:133003820-133003821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367642469	chr2:133003821-133003822	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142938774	chr2:133003824-133003825	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370793941	chr2:133003829-133003830	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375266802	chr2:133003831-133003832	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368294088	chr2:133003838-133003839	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372317123	chr2:133003840-133003841	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112746172	chr2:133003844-133003845	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375902617	chr2:133003847-133003848	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368745213	chr2:133003848-133003849	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372234559	chr2:133003849-133003850	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4402820	chr2:133003852-133003853	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576289305	chr2:133003853-133003854	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185879452	chr2:133003861-133003862	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145226787	chr2:133003863-133003864	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537330177	chr2:133003864-133003865	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374812086	chr2:133003865-133003866	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558830724	chr2:133003869-133003870	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368927040	chr2:133003874-133003875	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4261763	chr2:133003883-133003884	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148922290	chr2:133003884-133003885	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372846827	chr2:133003885-133003886	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201407898	chr2:133003890-133003891	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138924407	chr2:133003894-133003895	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200052247	chr2:133003903-133003904	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:132994800-133008800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr2:132994800-133009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:132995000-133005000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
4	chr2:132996000-133009800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr2:132996200-133005200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr2:132996200-133008600	ZNF genes & repeats	Primary T cells from cord blood	blood
7	chr2:133002200-133003800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr2:133002200-133003800	ZNF genes & repeats	Fetal Brain Male	brain
9	chr2:133002200-133004800	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
10	chr2:133002200-133009600	ZNF genes & repeats	Liver	Liver
11	chr2:133002200-133009800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
12	chr2:133002800-133003800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
13	chr2:133003000-133003800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
14	chr2:133003000-133003800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr2:133003000-133003800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:133003200-133003800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
17	chr2:133003200-133003800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:133003200-133006200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:133003200-133011000	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr2:133003600-133004400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr2:133003600-133004400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:133003600-133004400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr2:133003600-133004400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr2:133003600-133004400	Weak transcription	Brain Anterior Caudate	brain
25	chr2:133003600-133004400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:133003600-133004400	Weak transcription	Colonic Mucosa	Colon
27	chr2:133003600-133004400	Weak transcription	Colon Smooth Muscle	Colon
28	chr2:133003600-133004400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr2:133003600-133004400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:133003600-133004400	Weak transcription	HUVEC	blood vessel
31	chr2:133003600-133004600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:133003600-133004600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:133003600-133004600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:133003600-133004600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:133003600-133004600	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr2:133003600-133004600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr2:133003600-133004600	Weak transcription	Aorta	Aorta
38	chr2:133003600-133004600	Weak transcription	Fetal Heart	heart
39	chr2:133003600-133004600	Weak transcription	Left Ventricle	heart
40	chr2:133003600-133004600	Weak transcription	Ovary	ovary
41	chr2:133003600-133004600	Weak transcription	Psoas Muscle	Psoas
42	chr2:133003600-133004600	Weak transcription	Small Intestine	intestine
43	chr2:133003600-133004600	Weak transcription	Stomach Mucosa	stomach
44	chr2:133003600-133004600	Weak transcription	HSMMtube	muscle
45	chr2:133003600-133004600	Weak transcription	K562	blood
46	chr2:133003600-133004600	Weak transcription	NH-A	brain
47	chr2:133003800-133004600	Weak transcription	Fetal Brain Male	brain
48	chr2:133004400-133004800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:133004400-133004800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
50	chr2:133004400-133005000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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