Variant report

Variant	nsv874138
Chromosome Location	chr2:53114775-53218774
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	ARID3A	chr2:53161835-53161893	HepG2	liver:	n/a	n/a
2	ATF2	chr2:53124799-53125218	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:53161624-53162186	GM12878	blood:	n/a	n/a
4	ATF2	chr2:53161550-53162230	GM12878	blood:	n/a	n/a
5	ATF3	chr2:53161366-53162095	HCT-116	colon:	n/a	n/a
6	BATF	chr2:53166348-53166822	GM12878	blood:	n/a	n/a
7	BATF	chr2:53161569-53162046	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
8	BATF	chr2:53161603-53162043	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
9	BCL11A	chr2:53152851-53153076	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:53161743-53162072	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
11	BCL11A	chr2:53166415-53166672	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:53158346-53158507	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:53161550-53162089	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
14	BCL3	chr2:53161702-53162170	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
15	BHLHE40	chr2:53161740-53162175	GM12878	blood:	n/a	n/a
16	BRCA1	chr2:53160924-53162066	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr2:53161275-53162160	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:53161249-53162217	HCT-116	colon:	n/a	chr2:53162199-53162210
19	CEBPB	chr2:53122154-53122200	Hela-S3	cervix:	n/a	chr2:53122180-53122191
20	CEBPB	chr2:53161386-53161765	ECC-1	luminal epithelium:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
21	CEBPB	chr2:53183276-53183632	IMR90	lung:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
22	CEBPB	chr2:53145642-53146180	IMR90	lung:	n/a	chr2:53145956-53145969
23	CEBPB	chr2:53183277-53183618	Hela-S3	cervix:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
24	CEBPB	chr2:53191978-53192295	IMR90	lung:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
25	CEBPB	chr2:53161220-53162079	IMR90	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
26	CEBPB	chr2:53131722-53132000	Hela-S3	cervix:	n/a	chr2:53131973-53131984
27	CEBPB	chr2:53161347-53161796	A549	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
28	CEBPB	chr2:53177447-53177714	A549	lung:	n/a	chr2:53177576-53177587
29	CEBPB	chr2:53183274-53183631	HepG2	liver:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
30	CEBPB	chr2:53123918-53124240	A549	lung:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
31	CEBPB	chr2:53122020-53122313	A549	lung:	n/a	chr2:53122180-53122191
32	CEBPB	chr2:53123954-53124241	IMR90	lung:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
33	CEBPB	chr2:53191991-53192268	Hela-S3	cervix:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
34	CEBPB	chr2:53177578-53177595	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr2:53160531-53162111	Hela-S3	cervix:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
36	CEBPB	chr2:53161204-53162173	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
37	CEBPB	chr2:53161364-53161728	HepG2	liver:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
38	CEBPB	chr2:53191959-53192336	H1-hESC	embryonic stem cell:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
39	CEBPB	chr2:53183266-53183630	A549	lung:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
40	CEBPB	chr2:53160427-53162176	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
41	CEBPB	chr2:53161266-53162009	A549	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
42	CEBPB	chr2:53177429-53177688	HepG2	liver:	n/a	chr2:53177576-53177587
43	CEBPB	chr2:53177426-53177727	IMR90	lung:	n/a	chr2:53177576-53177587
44	CEBPB	chr2:53145768-53146137	Hela-S3	cervix:	n/a	chr2:53145956-53145969
45	CEBPB	chr2:53122149-53122189	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:53155376-53155506	A549	lung:	n/a	n/a
47	CEBPB	chr2:53161339-53161782	ECC-1	luminal epithelium:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
48	CEBPB	chr2:53161558-53162223	GM12878	blood:	n/a	chr2:53161857-53161869
49	CEBPB	chr2:53123913-53124233	HepG2	liver:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
50	CEBPB	chr2:53191970-53192319	A549	lung:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53192311-53192361	BJ	skin:	n/a
2	chr2:53160678-53160728	H1-hESC	embryonic stem cell:	embryo
3	chr2:53160678-53160728	U87	brain:	n/a
4	chr2:53160678-53160728	SAEC	small airway:	n/a
5	chr2:53192311-53192361	HL-60	blood:	n/a
6	chr2:53160678-53160728	AG09319	gingival:	n/a
7	chr2:53160678-53160728	A549	lung:	n/a
8	chr2:53160678-53160728	AG10803	skin:	n/a
9	chr2:53192311-53192361	SAEC	small airway:	n/a
10	chr2:53160678-53160728	GM12891	blood:	n/a
11	chr2:53192311-53192361	HUVEC	blood vessel:	n/a
12	chr2:53160678-53160728	GM19239	blood:	n/a
13	chr2:53160678-53160728	BJ	skin:	n/a
14	chr2:53160678-53160728	T-47D	breast:	n/a
15	chr2:53160678-53160728	Caco-2	colon:	n/a
16	chr2:53192311-53192361	HAEpiC	amniotic membrane:	n/a
17	chr2:53192311-53192361	GM12878	blood:	n/a
18	chr2:53192311-53192361	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:53192311-53192361	ECC-1	luminal epithelium:	n/a
20	chr2:53192311-53192361	NT2-D1	testis:	n/a
21	chr2:53160678-53160728	HCT-116	colon:	n/a
22	chr2:53192311-53192361	HRE	kidney:	n/a
23	chr2:53192311-53192361	SKMC	muscle:	n/a
24	chr2:53160678-53160728	Hepatocyte	liver:	n/a
25	chr2:53192311-53192361	NH-A	brain:	n/a
26	chr2:53160678-53160728	CMK	blood:	n/a
27	chr2:53192311-53192361	K562	blood:	n/a
28	chr2:53192311-53192361	SK-N-SH_RA	brain:	n/a
29	chr2:53160678-53160728	GM06990	blood:	n/a
30	chr2:53192311-53192361	AG10803	skin:	n/a
31	chr2:53160678-53160728	HRCEpiC	kidney:	n/a
32	chr2:53192311-53192361	T-47D	breast:	n/a
33	chr2:53160678-53160728	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:53160678-53160728	MCF-7	breast:	n/a
35	chr2:53160678-53160728	HIPEpiC	eye:	n/a
36	chr2:53160678-53160728	SK-N-SH	brain:	n/a
37	chr2:53160678-53160728	LNCaP	prostate:	n/a
38	chr2:53192311-53192361	HCM	heart:	n/a
39	chr2:53192311-53192361	HEK293	kidney:	embryo
40	chr2:53192311-53192361	HRPEpiC	eye:	n/a
41	chr2:53160678-53160728	HNPCEpiC	eye:	n/a
42	chr2:53192311-53192361	BE2_C	brain:	n/a
43	chr2:53192311-53192361	GM12892	blood:	n/a
44	chr2:53160678-53160728	AG04449	skin:	fetal
45	chr2:53192311-53192361	AG09319	gingival:	n/a
46	chr2:53192311-53192361	H1-hESC	embryonic stem cell:	embryo
47	chr2:53160678-53160728	HCM	heart:	n/a
48	chr2:53160678-53160728	HMEC	breast:	n/a
49	chr2:53160678-53160728	ECC-1	luminal epithelium:	n/a
50	chr2:53160678-53160728	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53037286..53038157-chr2:53203093..53203814,3	MCF-7	breast:
2	chr2:53198477..53200410-chr2:53204167..53206396,2	K562	blood:
3	chr2:53203292..53203812-chr2:53700344..53701275,2	MCF-7	breast:
4	chr2:53198477..53200410-chr2:53204167..53206396,2	K562	blood:
5	chr2:53048846..53049807-chr2:53183875..53184416,2	MCF-7	breast:
6	chr2:53115077..53117448-chr2:53686034..53688851,2	MCF-7	breast:
7	chr2:53132852..53133808-chr20:52198265..52198765,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
2	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033
3	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
4	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033

Variant related genes	Relation type
ENSG00000228033	TF binding region
ENSG00000228033	CpG island

Extended variants
information (count: 3688 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3688 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2048309	chr2:53114775-53114776	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191105969	chr2:53114785-53114786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544228486	chr2:53114809-53114810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564199871	chr2:53114820-53114821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562420059	chr2:53114856-53114857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35687660	chr2:53114875-53114876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551132156	chr2:53114884-53114885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72900364	chr2:53114915-53114916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532225576	chr2:53114959-53114960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373690666	chr2:53114960-53114961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551866102	chr2:53114961-53114962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148167917	chr2:53114966-53114967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182771983	chr2:53115002-53115003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78638626	chr2:53115032-53115033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568331565	chr2:53115056-53115057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373143764	chr2:53115060-53115061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187245855	chr2:53115088-53115089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191273086	chr2:53115094-53115095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182314957	chr2:53115097-53115098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570562437	chr2:53115150-53115151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs207461766	chr2:53115163-53115164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59114690	chr2:53115176-53115177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546353381	chr2:53115180-53115181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532046182	chr2:53115181-53115182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78522067	chr2:53115202-53115203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56286124	chr2:53115203-53115204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571885815	chr2:53115231-53115232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187894434	chr2:53115260-53115261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529101942	chr2:53115290-53115291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193296157	chr2:53115345-53115346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549058699	chr2:53115382-53115383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575890309	chr2:53115391-53115392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544617325	chr2:53115434-53115435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533031834	chr2:53115451-53115452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564663026	chr2:53115470-53115471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185110359	chr2:53115515-53115516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143950702	chr2:53115558-53115559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545464864	chr2:53115570-53115571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559040293	chr2:53115577-53115578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528208898	chr2:53115597-53115598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546704763	chr2:53115616-53115617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144778226	chr2:53115617-53115618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548150036	chr2:53115624-53115625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190352139	chr2:53115626-53115627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568012760	chr2:53115684-53115685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530791418	chr2:53115689-53115690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146748477	chr2:53115690-53115691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192949394	chr2:53115707-53115708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539657640	chr2:53115727-53115728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553238565	chr2:53115745-53115746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
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

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53105600-53121800	Weak transcription	Pancreas	Pancrea
2	chr2:53108200-53119800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:53109200-53115800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:53109400-53145600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:53115800-53117200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:53119800-53120200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:53120200-53121200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:53121200-53121600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:53121200-53122200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:53121800-53122000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:53121800-53122000	ZNF genes & repeats	Pancreas	Pancrea
12	chr2:53122000-53122200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr2:53122000-53122400	Weak transcription	Pancreas	Pancrea
14	chr2:53122200-53126200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:53123200-53125200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:53124000-53126000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr2:53124600-53124800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:53124800-53126000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:53125800-53126400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:53126000-53126200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:53126000-53126400	ZNF genes & repeats	Gastric	stomach
22	chr2:53126200-53126400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:53131400-53131800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:53131400-53132000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:53131400-53132000	Enhancers	Fetal Muscle Leg	muscle
26	chr2:53131400-53132400	Enhancers	Hela-S3	cervix
27	chr2:53144200-53144400	Enhancers	Fetal Intestine Large	intestine
28	chr2:53144200-53144400	Enhancers	Hela-S3	cervix
29	chr2:53144400-53145400	Weak transcription	Hela-S3	cervix
30	chr2:53145400-53146000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:53145400-53147000	Enhancers	Hela-S3	cervix
32	chr2:53145400-53147200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:53145400-53147200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr2:53145600-53146200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:53145600-53146400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:53145600-53147200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:53146400-53147200	Enhancers	Fetal Intestine Small	intestine
38	chr2:53146400-53148000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr2:53146400-53160000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:53146800-53147000	Enhancers	Fetal Intestine Large	intestine
41	chr2:53147000-53147600	Enhancers	Stomach Mucosa	stomach
42	chr2:53156600-53157400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:53157200-53157800	Weak transcription	Aorta	Aorta
44	chr2:53157400-53158600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:53158600-53159200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:53158600-53159200	Enhancers	GM12878-XiMat	blood
47	chr2:53158800-53159200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:53159200-53160000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:53159200-53160400	Weak transcription	GM12878-XiMat	blood
50	chr2:53159200-53162200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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