Variant report

Variant	nsv874126
Chromosome Location	chr2:52783672-52841595
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	CEBPB	chr2:52796334-52796619	A549	lung:	n/a	chr2:52796497-52796508
2	CEBPB	chr2:52796324-52796609	HepG2	liver:	n/a	chr2:52796497-52796508
3	CEBPB	chr2:52834371-52834680	HepG2	liver:	n/a	chr2:52834518-52834527 chr2:52834516-52834527 chr2:52834517-52834528 chr2:52834518-52834527 chr2:52834518-52834527 chr2:52834518-52834527
4	CEBPB	chr2:52834381-52834700	K562	blood:	n/a	chr2:52834518-52834527 chr2:52834516-52834527 chr2:52834517-52834528 chr2:52834518-52834527 chr2:52834518-52834527 chr2:52834518-52834527
5	CEBPB	chr2:52805150-52805325	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:52841343-52841411	A549	lung:	n/a	n/a
7	CEBPB	chr2:52796338-52796610	IMR90	lung:	n/a	chr2:52796497-52796508
8	CEBPB	chr2:52834390-52834658	IMR90	lung:	n/a	chr2:52834518-52834527 chr2:52834516-52834527 chr2:52834517-52834528 chr2:52834518-52834527 chr2:52834518-52834527 chr2:52834518-52834527
9	CTCF	chr2:52840325-52840500	MCF-7	breast:	n/a	chr2:52840412-52840430
10	CTCF	chr2:52840360-52840510	HCPEpiC	choroid plexus:	n/a	chr2:52840412-52840430
11	CTCF	chr2:52840295-52840495	GM12878	blood:	n/a	chr2:52840412-52840430
12	CTCF	chr2:52819216-52819219	GM10248	blood:	n/a	n/a
13	CTCF	chr2:52840340-52840490	MCF-7	breast:	n/a	chr2:52840412-52840430
14	CTCF	chr2:52840320-52840470	HBMEC	blood vessel:	n/a	chr2:52840412-52840430
15	CTCF	chr2:52840280-52840430	HAc	cerebellar:	n/a	chr2:52840412-52840430
16	CTCF	chr2:52840397-52840465	HUVEC	blood vessel:	n/a	chr2:52840412-52840430
17	CTCF	chr2:52840320-52840470	HPAF	blood vessel:	n/a	chr2:52840412-52840430
18	CTCF	chr2:52840349-52840416	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:52840360-52840510	SK-N-SH_RA	brain:	n/a	chr2:52840412-52840430
20	CTCF	chr2:52840220-52840370	HMF	breast:	n/a	n/a
21	CTCF	chr2:52840342-52840516	LNCaP	prostate:	n/a	chr2:52840412-52840430
22	CTCF	chr2:52840282-52840600	IMR90	lung:	n/a	chr2:52840412-52840430
23	CTCF	chr2:52840340-52840490	WERI-Rb-1	eye:	n/a	chr2:52840412-52840430
24	CTCF	chr2:52807056-52807087	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:52840340-52840490	HA-sp	spinal cord:	n/a	chr2:52840412-52840430
26	CTCF	chr2:52840400-52840550	A549	lung:	n/a	chr2:52840412-52840430
27	CTCF	chr2:52840340-52840490	NB4	blood:	n/a	chr2:52840412-52840430
28	CTCF	chr2:52840371-52840464	HepG2	liver:	n/a	chr2:52840412-52840430
29	CTCF	chr2:52840340-52840490	HCPEpiC	choroid plexus:	n/a	chr2:52840412-52840430
30	CTCF	chr2:52840340-52840490	HCM	heart:	n/a	chr2:52840412-52840430
31	CTCF	chr2:52840360-52840510	HPF	lung:	n/a	chr2:52840412-52840430
32	CTCF	chr2:52840375-52840439	NHEK	skin:	n/a	chr2:52840412-52840430
33	CTCF	chr2:52840317-52840514	Hela-S3	cervix:	n/a	chr2:52840412-52840430
34	CTCF	chr2:52840320-52840470	BE2_C	brain:	n/a	chr2:52840412-52840430
35	CTCF	chr2:52840228-52840664	HCT-116	colon:	n/a	chr2:52840412-52840430
36	CTCF	chr2:52840293-52840526	Gliobla	brain:	n/a	chr2:52840412-52840430
37	CTCF	chr2:52840308-52840494	A549	lung:	n/a	chr2:52840412-52840430
38	CTCF	chr2:52840369-52840451	H1-hESC	embryonic stem cell:	n/a	chr2:52840412-52840430
39	CTCF	chr2:52785300-52785450	GM12866	blood:	n/a	n/a
40	CTCF	chr2:52840292-52840663	MCF-7	breast:	n/a	chr2:52840412-52840430
41	CTCF	chr2:52840343-52840467	MCF-7	breast:	n/a	chr2:52840412-52840430
42	CTCF	chr2:52840360-52840510	SAEC	small airway:	n/a	chr2:52840412-52840430
43	CTCF	chr2:52840400-52840550	RPTEC	kidney:	n/a	chr2:52840412-52840430
44	CTCF	chr2:52840340-52840490	Caco-2	colon:	n/a	chr2:52840412-52840430
45	CTCF	chr2:52840224-52840534	H1-hESC	embryonic stem cell:	n/a	chr2:52840412-52840430
46	CTCF	chr2:52840340-52840490	HRPEpiC	eye:	n/a	chr2:52840412-52840430
47	CTCF	chr2:52840300-52840450	HMEC	breast:	n/a	chr2:52840412-52840430
48	CTCF	chr2:52840360-52840510	HCT-116	colon:	n/a	chr2:52840412-52840430
49	CTCF	chr2:52840354-52840449	ProgFib	skin:	n/a	chr2:52840412-52840430
50	CTCF	chr2:52840201-52840646	MCF-7	breast:	n/a	chr2:52840412-52840430

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52798363-52798413	ECC-1	luminal epithelium:	n/a
2	chr2:52798363-52798413	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:52798363-52798413	ECC-1	luminal epithelium:	n/a
4	chr2:52798363-52798413	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:52785721-52785771	GM19239	blood:	n/a
6	chr2:52799970-52800020	AG04450	lung:	fetal
7	chr2:52799518-52799568	PrEC	prostate:	n/a
8	chr2:52798363-52798413	NH-A	brain:	n/a
9	chr2:52798801-52798851	HIPEpiC	eye:	n/a
10	chr2:52798801-52798851	BJ	skin:	n/a
11	chr2:52798363-52798413	ProgFib	skin:	n/a
12	chr2:52799970-52800020	AG04449	skin:	fetal
13	chr2:52796128-52796178	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:52802050-52802100	SK-N-MC	brain:	n/a
15	chr2:52799378-52799428	PFSK-1	brain:	n/a
16	chr2:52799378-52799428	Hepatocyte	liver:	n/a
17	chr2:52799378-52799428	HAEpiC	amniotic membrane:	n/a
18	chr2:52799970-52800020	AG09309	skin:	n/a
19	chr2:52798801-52798851	Hela-S3	cervix:	n/a
20	chr2:52785721-52785771	HL-60	blood:	n/a
21	chr2:52799378-52799428	SKMC	muscle:	n/a
22	chr2:52799518-52799568	RPTEC	kidney:	n/a
23	chr2:52799518-52799568	NH-A	brain:	n/a
24	chr2:52799378-52799428	NHDF-neo	bronchial:	n/a
25	chr2:52802050-52802100	AG09319	gingival:	n/a
26	chr2:52799378-52799428	HEEpiC	esophagus:	n/a
27	chr2:52785721-52785771	HCPEpiC	choroid plexus:	n/a
28	chr2:52798801-52798851	PrEC	prostate:	n/a
29	chr2:52799378-52799428	AG09309	skin:	n/a
30	chr2:52799970-52800020	SK-N-SH_RA	brain:	n/a
31	chr2:52799378-52799428	HCPEpiC	choroid plexus:	n/a
32	chr2:52797873-52797923	Jurkat	blood:	n/a
33	chr2:52785721-52785771	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:52798927-52798977	IMR90	lung:	fetal
35	chr2:52799378-52799428	IMR90	lung:	fetal
36	chr2:52796128-52796178	AG09309	skin:	n/a
37	chr2:52798363-52798413	A549	lung:	n/a
38	chr2:52798801-52798851	HCF	heart:	n/a
39	chr2:52796128-52796178	ECC-1	luminal epithelium:	n/a
40	chr2:52796128-52796178	SKMC	muscle:	n/a
41	chr2:52798363-52798413	HRPEpiC	eye:	n/a
42	chr2:52798927-52798977	AoSMC	blood vessel:	n/a
43	chr2:52785721-52785771	NB4	blood:	n/a
44	chr2:52798363-52798413	HEK293	kidney:	embryo
45	chr2:52799378-52799428	AoSMC	blood vessel:	n/a
46	chr2:52799518-52799568	HEEpiC	esophagus:	n/a
47	chr2:52785721-52785771	NH-A	brain:	n/a
48	chr2:52796128-52796178	HRCEpiC	kidney:	n/a
49	chr2:52799518-52799568	PANC-1	pancreas:	n/a
50	chr2:52802050-52802100	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52644535..52645157-chr2:52839947..52840842,2	MCF-7	breast:
2	chr2:52840541..52843528-chr2:52846569..52849939,3	K562	blood:
3	chr2:52796228..52798842-chr2:52811268..52813785,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000204993	TF binding region
ENSG00000204993	CpG island
ENSG00000204993	chromatin interactions

Extended variants
information (count: 1383 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538080493	chr2:52784640-52784641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557906728	chr2:52784660-52784661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571652964	chr2:52784724-52784725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144578326	chr2:52784746-52784747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188451994	chr2:52784759-52784760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13416351	chr2:52784796-52784797	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs115767176	chr2:52784837-52784838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148511479	chr2:52784841-52784842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555536421	chr2:52784857-52784858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575389919	chr2:52784866-52784867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534992244	chr2:52784875-52784876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372518291	chr2:52784907-52784908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12478397	chr2:52784952-52784953	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs62127644	chr2:52784966-52784967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564265870	chr2:52785002-52785003	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142766019	chr2:52785004-52785005	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs192281124	chr2:52785020-52785021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183837683	chr2:52785059-52785060	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs541425255	chr2:52785081-52785082	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560309486	chr2:52785104-52785105	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs376208358	chr2:52785131-52785132	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs529255561	chr2:52785134-52785135	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs151070590	chr2:52785142-52785143	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569035273	chr2:52785211-52785212	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs189293049	chr2:52785232-52785233	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140797752	chr2:52785233-52785234	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571465623	chr2:52785234-52785235	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs79204973	chr2:52785256-52785257	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs143635587	chr2:52785270-52785271	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554417589	chr2:52785290-52785291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566360191	chr2:52785308-52785309	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs6749593	chr2:52785320-52785321	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555400135	chr2:52785324-52785325	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113050947	chr2:52785375-52785376	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs60177040	chr2:52785379-52785380	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs557989736	chr2:52785398-52785399	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7584416	chr2:52785407-52785408	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs540175582	chr2:52785415-52785416	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs111789648	chr2:52785446-52785447	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs560434585	chr2:52785450-52785451	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs6545286	chr2:52785456-52785457	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs528626803	chr2:52785496-52785497	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369159718	chr2:52785528-52785529	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs562531707	chr2:52785532-52785533	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs562523333	chr2:52785546-52785547	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs373921411	chr2:52785551-52785552	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6545287	chr2:52785554-52785555	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565359473	chr2:52785566-52785567	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs60635030	chr2:52785576-52785577	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs370109335	chr2:52785602-52785603	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52784600-52785000	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr2:52784600-52786200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:52784800-52786200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:52784800-52786400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:52785000-52785200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:52785000-52785400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr2:52785000-52786200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:52785200-52785400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:52785200-52785600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr2:52785200-52785800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:52785200-52785800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr2:52785200-52786000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:52785200-52786000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr2:52785400-52785600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:52785400-52785600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:52785400-52785800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:52785400-52785800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:52785400-52785800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:52785600-52785800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr2:52785600-52786000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:52785600-52795200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:52785800-52786200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr2:52785800-52790000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:52786000-52786200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:52790000-52790200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:52790200-52790800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:52790800-52791000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:52791000-52791200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:52791200-52792400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:52798000-52798600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:52798000-52799600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr2:52798000-52800000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:52807400-52807800	Enhancers	Fetal Lung	lung
34	chr2:52811800-52813000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:52812600-52813200	Enhancers	Dnd41	blood
36	chr2:52813200-52819200	Weak transcription	Dnd41	blood
37	chr2:52813600-52814000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr2:52819200-52819600	ZNF genes & repeats	Dnd41	blood
39	chr2:52819600-52821200	Weak transcription	Dnd41	blood
40	chr2:52820600-52820800	Enhancers	HUVEC	blood vessel
41	chr2:52821000-52821400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr2:52821000-52821600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:52821000-52821600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr2:52821200-52821600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:52821200-52821600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:52821200-52821600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr2:52821200-52821600	Active TSS	Brain Hippocampus Middle	brain
48	chr2:52821200-52821800	Enhancers	Fetal Kidney	kidney
49	chr2:52821200-52822000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr2:52821200-52823000	Enhancers	Dnd41	blood

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