Variant report

Variant	esv2762447
Chromosome Location	chr2:33643724-33674484
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:306)
Chromatin interactive
region (count:17)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 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	chr2:33662375-33662635	K562	blood:	n/a	n/a
2	ATF1	chr2:33670294-33670411	K562	blood:	n/a	n/a
3	ATF1	chr2:33664269-33664530	K562	blood:	n/a	n/a
4	ATF1	chr2:33662358-33662742	K562	blood:	n/a	n/a
5	ATF1	chr2:33657024-33657225	K562	blood:	n/a	n/a
6	BACH1	chr2:33661484-33661493	K562	blood:	n/a	n/a
7	BHLHE40	chr2:33666338-33666658	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:33646309-33646320	K562	blood:	n/a	n/a
9	BHLHE40	chr2:33651830-33651942	K562	blood:	n/a	n/a
10	BHLHE40	chr2:33662643-33662683	K562	blood:	n/a	n/a
11	CBX3	chr2:33666217-33666655	K562	blood:	n/a	n/a
12	CBX3	chr2:33662398-33662787	K562	blood:	n/a	n/a
13	CCNT2	chr2:33662482-33662759	K562	blood:	n/a	n/a
14	CEBPB	chr2:33650621-33650921	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:33658377-33658699	A549	lung:	n/a	chr2:33658516-33658527 chr2:33658665-33658678
16	CEBPB	chr2:33673645-33673978	IMR90	lung:	n/a	chr2:33673811-33673822
17	CEBPB	chr2:33658412-33658650	H1-hESC	embryonic stem cell:	n/a	chr2:33658516-33658527
18	CEBPB	chr2:33658340-33658710	K562	blood:	n/a	chr2:33658665-33658678 chr2:33658516-33658527
19	CEBPB	chr2:33673672-33673914	H1-hESC	embryonic stem cell:	n/a	chr2:33673811-33673822
20	CEBPB	chr2:33658343-33658709	IMR90	lung:	n/a	chr2:33658665-33658678 chr2:33658516-33658527
21	CEBPB	chr2:33667926-33668010	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:33658345-33658698	HepG2	liver:	n/a	chr2:33658665-33658678 chr2:33658516-33658527
23	CEBPB	chr2:33673642-33673982	HepG2	liver:	n/a	chr2:33673811-33673822
24	CEBPB	chr2:33658379-33658682	K562	blood:	n/a	chr2:33658665-33658678 chr2:33658516-33658527
25	CEBPB	chr2:33656200-33656454	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:33673681-33673938	K562	blood:	n/a	chr2:33673811-33673822
27	CEBPB	chr2:33673691-33673945	Hela-S3	cervix:	n/a	chr2:33673811-33673822
28	CEBPB	chr2:33668336-33668676	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:33662335-33662641	IMR90	lung:	n/a	n/a
30	CEBPD	chr2:33662366-33662855	K562	blood:	n/a	n/a
31	CHD1	chr2:33662127-33663255	IMR90	lung:	n/a	n/a
32	CHD2	chr2:33666469-33666530	K562	blood:	n/a	n/a
33	CTCF	chr2:33645600-33645750	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr2:33666420-33666570	GM12866	blood:	n/a	chr2:33666483-33666501
35	CTCF	chr2:33666440-33666590	RPTEC	kidney:	n/a	chr2:33666483-33666501
36	CTCF	chr2:33666440-33666590	GM12874	blood:	n/a	chr2:33666483-33666501
37	CTCF	chr2:33666400-33666550	HepG2	liver:	n/a	chr2:33666483-33666501
38	CTCF	chr2:33666440-33666590	NHDF-neo	bronchial:	n/a	chr2:33666483-33666501
39	CTCF	chr2:33644720-33644870	HepG2	liver:	n/a	n/a
40	CTCF	chr2:33666420-33666570	GM12869	blood:	n/a	chr2:33666483-33666501
41	CTCF	chr2:33644720-33644870	HVMF	connective:	n/a	n/a
42	CTCF	chr2:33666385-33666623	ProgFib	skin:	n/a	chr2:33666483-33666501
43	CTCF	chr2:33644740-33644890	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr2:33645500-33645650	HAc	cerebellar:	n/a	n/a
45	CTCF	chr2:33666420-33666570	HMEC	breast:	n/a	chr2:33666483-33666501
46	CTCF	chr2:33644720-33644870	HEK293	kidney:	n/a	n/a
47	CTCF	chr2:33666378-33666602	LNCaP	prostate:	n/a	chr2:33666483-33666501
48	CTCF	chr2:33666386-33666635	GM13977	blood:	n/a	chr2:33666483-33666501
49	CTCF	chr2:33666420-33666570	GM12873	blood:	n/a	chr2:33666483-33666501
50	CTCF	chr2:33666440-33666590	AG04449	skin:	n/a	chr2:33666483-33666501

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33645526-33645576	A549	lung:	n/a
2	chr2:33645526-33645576	A549	lung:	n/a
3	chr2:33645526-33645576	Hela-S3	cervix:	n/a
4	chr2:33660754-33660804	HEK293	kidney:	embryo
5	chr2:33660672-33660722	SK-N-SH	brain:	n/a
6	chr2:33652047-33652097	HRPEpiC	eye:	n/a
7	chr2:33660754-33660804	HCF	heart:	n/a
8	chr2:33660754-33660804	HepG2	liver:	n/a
9	chr2:33645526-33645576	ProgFib	skin:	n/a
10	chr2:33652047-33652097	ProgFib	skin:	n/a
11	chr2:33645526-33645576	HEK293	kidney:	embryo
12	chr2:33652047-33652097	HCT-116	colon:	n/a
13	chr2:33652047-33652097	SKMC	muscle:	n/a
14	chr2:33661362-33661412	PANC-1	pancreas:	n/a
15	chr2:33652047-33652097	CMK	blood:	n/a
16	chr2:33645526-33645576	K562	blood:	n/a
17	chr2:33660672-33660722	MCF-7	breast:	n/a
18	chr2:33661362-33661412	HEK293	kidney:	embryo
19	chr2:33645526-33645576	H1-hESC	embryonic stem cell:	embryo
20	chr2:33652047-33652097	NHBE	bronchial:	n/a
21	chr2:33645526-33645576	Caco-2	colon:	n/a
22	chr2:33660672-33660722	AG09309	skin:	n/a
23	chr2:33660754-33660804	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:33652047-33652097	GM06990	blood:	n/a
25	chr2:33660754-33660804	A549	lung:	n/a
26	chr2:33661362-33661412	GM12891	blood:	n/a
27	chr2:33652047-33652097	AoSMC	blood vessel:	n/a
28	chr2:33652047-33652097	NH-A	brain:	n/a
29	chr2:33661362-33661412	PFSK-1	brain:	n/a
30	chr2:33652047-33652097	AG10803	skin:	n/a
31	chr2:33652047-33652097	HCF	heart:	n/a
32	chr2:33652047-33652097	GM12878	blood:	n/a
33	chr2:33660754-33660804	SK-N-SH_RA	brain:	n/a
34	chr2:33660754-33660804	NB4	blood:	n/a
35	chr2:33660754-33660804	HCT-116	colon:	n/a
36	chr2:33645526-33645576	ovcar-3	ovarian:	n/a
37	chr2:33661362-33661412	AoSMC	blood vessel:	n/a
38	chr2:33660672-33660722	NHDF-neo	bronchial:	n/a
39	chr2:33660672-33660722	HIPEpiC	eye:	n/a
40	chr2:33660754-33660804	SAEC	small airway:	n/a
41	chr2:33660754-33660804	NT2-D1	testis:	n/a
42	chr2:33660754-33660804	NH-A	brain:	n/a
43	chr2:33661362-33661412	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:33660672-33660722	HCT-116	colon:	n/a
45	chr2:33660672-33660722	HepG2	liver:	n/a
46	chr2:33660672-33660722	ovcar-3	ovarian:	n/a
47	chr2:33660672-33660722	HEK293	kidney:	embryo
48	chr2:33660672-33660722	HRE	kidney:	n/a
49	chr2:33660672-33660722	HUVEC	blood vessel:	n/a
50	chr2:33661362-33661412	ProgFib	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:33645952..33647644-chr2:33651706..33654003,2	MCF-7	breast:
2	chr2:33645952..33647644-chr2:33651706..33654003,2	MCF-7	breast:
3	chr2:33638138..33638651-chr2:33665997..33666555,2	MCF-7	breast:
4	chr2:33644817..33647269-chr2:33650448..33652566,2	K562	blood:
5	chr2:33665492..33668355-chr2:33669138..33671096,3	K562	blood:
6	chr2:33645116..33647269-chr2:33650448..33653137,2	K562	blood:
7	chr2:33645116..33647269-chr2:33650448..33653137,2	K562	blood:
8	chr2:33650872..33654290-chr2:33656071..33658899,3	K562	blood:
9	chr2:33662537..33665066-chr2:33668209..33670652,2	K562	blood:
10	chr2:33650872..33654290-chr2:33656071..33658899,3	K562	blood:
11	chr2:33660258..33662233-chr2:33665386..33666993,2	K562	blood:
12	chr2:33662537..33665066-chr2:33668209..33670652,2	K562	blood:
13	chr2:33644817..33647269-chr2:33650448..33652566,2	K562	blood:
14	chr2:33259626..33260439-chr2:33665962..33666763,2	MCF-7	breast:
15	chr2:33660258..33665066-chr2:33665386..33670652,5	K562	blood:
16	chr2:33669708..33670407-chr3:131810762..131811621,2	MCF-7	breast:
17	chr2:33665492..33668355-chr2:33669138..33671096,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTBP1-1	chr2:33661393-33661658	NONHSAT070011
2	lnc-LTBP1-1	chr2:33661480-33661658	NONHSAT070012
3	lnc-LTBP1-1	chr2:33672887-33673010	NONHSAT070012
4	lnc-LTBP1-1	chr2:33672887-33673010	NONHSAT070011

No data

Variant related genes	Relation type
RASGRP3	TF binding region
RASGRP3	CpG island
ENSG00000152689	chromatin interactions

Extended variants
information (count: 1426 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1426 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6724875	chr2:33643740-33643741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367878507	chr2:33643744-33643745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76703549	chr2:33643745-33643746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181631487	chr2:33643768-33643769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564719635	chr2:33643772-33643773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116276045	chr2:33643774-33643775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186255951	chr2:33643793-33643794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145979476	chr2:33643801-33643802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139853348	chr2:33643806-33643807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386644600	chr2:33643807-33643808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548703073	chr2:33643808-33643809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368714228	chr2:33643818-33643819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568793439	chr2:33643820-33643821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531345461	chr2:33643850-33643851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182508384	chr2:33643857-33643858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571136845	chr2:33643862-33643863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533723420	chr2:33643883-33643884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377590359	chr2:33643889-33643890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112499213	chr2:33643893-33643894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553523612	chr2:33643904-33643905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143234057	chr2:33643911-33643912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370643560	chr2:33643923-33643924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555519481	chr2:33643958-33643959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187141116	chr2:33644007-33644008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146729072	chr2:33644016-33644017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558270493	chr2:33644026-33644027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547013431	chr2:33644072-33644073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375838058	chr2:33644074-33644075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115433604	chr2:33644115-33644116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540848775	chr2:33644116-33644117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560619069	chr2:33644128-33644129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148443342	chr2:33644143-33644144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533081197	chr2:33644171-33644172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562390137	chr2:33644183-33644184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74875822	chr2:33644189-33644190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372314967	chr2:33644269-33644270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142743427	chr2:33644278-33644279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115142250	chr2:33644356-33644357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111975075	chr2:33644357-33644358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527339314	chr2:33644382-33644383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552572357	chr2:33644415-33644416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547200131	chr2:33644484-33644485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114184452	chr2:33644507-33644508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115229049	chr2:33644516-33644517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111267824	chr2:33644568-33644569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556402955	chr2:33644571-33644572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191099098	chr2:33644594-33644595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538256371	chr2:33644650-33644651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182350531	chr2:33644651-33644652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578144777	chr2:33644715-33644716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Pancreatic cancer	17952125	CNVD
Autism	22495309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33634000-33645000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:33637600-33645000	Weak transcription	NHLF	lung
3	chr2:33637800-33645000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:33638200-33645000	Weak transcription	HSMM	muscle
5	chr2:33638200-33645400	Weak transcription	HSMMtube	muscle
6	chr2:33638600-33644600	Weak transcription	A549	lung
7	chr2:33638600-33644800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:33640200-33651400	Weak transcription	Fetal Heart	heart
9	chr2:33642000-33645200	Weak transcription	Left Ventricle	heart
10	chr2:33642200-33646000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr2:33642400-33650400	Weak transcription	NHDF-Ad	bronchial
12	chr2:33642600-33644400	Weak transcription	HUVEC	blood vessel
13	chr2:33642600-33644800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:33642600-33644800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:33642600-33645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:33642600-33645400	Weak transcription	NH-A	brain
17	chr2:33644400-33645800	Enhancers	Fetal Kidney	kidney
18	chr2:33644400-33646600	Enhancers	HUVEC	blood vessel
19	chr2:33644600-33645400	Enhancers	A549	lung
20	chr2:33644800-33645200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:33644800-33646400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:33644800-33646400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:33644800-33646400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:33645000-33645200	Enhancers	NHLF	lung
25	chr2:33645000-33645400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:33645000-33645400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:33645000-33645400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:33645000-33646200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:33645000-33646200	Enhancers	Fetal Muscle Leg	muscle
30	chr2:33645000-33646400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:33645000-33646400	Enhancers	HSMM	muscle
32	chr2:33645200-33645400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:33645200-33646200	Enhancers	Left Ventricle	heart
34	chr2:33645200-33650600	Weak transcription	NHLF	lung
35	chr2:33645200-33667800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:33645400-33645600	Weak transcription	Placenta	Placenta
37	chr2:33645400-33646200	Enhancers	Fetal Thymus	thymus
38	chr2:33645400-33646400	Enhancers	HSMMtube	muscle
39	chr2:33645400-33646400	Enhancers	NH-A	brain
40	chr2:33645400-33650200	Weak transcription	A549	lung
41	chr2:33645600-33645800	Enhancers	Placenta	Placenta
42	chr2:33645800-33647000	Weak transcription	Placenta	Placenta
43	chr2:33645800-33647800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr2:33645800-33661200	Weak transcription	Fetal Kidney	kidney
45	chr2:33646000-33646400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr2:33646400-33646800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:33646400-33650200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:33646400-33650400	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr2:33646400-33650400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr2:33646400-33650400	Weak transcription	NH-A	brain

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