Variant report

Variant	esv2753082
Chromosome Location	chr2:73891045-73955545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:490)
Chromatin interactive
region (count:30)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73944205-73944414	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
4	ATF1	chr2:73943828-73944353	K562	blood:	n/a	n/a
5	ATF1	chr2:73928292-73928546	K562	blood:	n/a	n/a
6	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
7	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
8	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
10	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
11	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
12	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
14	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:73928154-73928613	K562	blood:	n/a	n/a
16	BHLHE40	chr2:73933790-73934083	K562	blood:	n/a	n/a
17	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
18	CBX3	chr2:73928047-73928946	K562	blood:	n/a	n/a
19	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
20	CBX3	chr2:73944839-73945197	K562	blood:	n/a	n/a
21	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
22	CBX3	chr2:73943935-73944537	K562	blood:	n/a	n/a
23	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
24	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
26	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
27	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
29	CEBPB	chr2:73940735-73940928	K562	blood:	n/a	chr2:73940777-73940788
30	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
31	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
32	CEBPB	chr2:73940681-73941130	A549	lung:	n/a	chr2:73940777-73940788
33	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
34	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
35	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
36	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73940714-73941127	IMR90	lung:	n/a	chr2:73940777-73940788
38	CEBPB	chr2:73940640-73941075	HepG2	liver:	n/a	chr2:73940777-73940788
39	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
40	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
41	CTCF	chr2:73907392-73907608	Spleen_OC	spleen:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
42	CTCF	chr2:73907290-73907291	ProgFib	skin:	n/a	n/a
43	CTCF	chr2:73907400-73907550	GM12878	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73907440-73907590	HFF	foreskin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
45	CTCF	chr2:73917940-73918090	WI-38	lung:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
46	CTCF	chr2:73907360-73907510	HMEC	breast:	n/a	n/a
47	CTCF	chr2:73907387-73907644	A549	lung:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
48	CTCF	chr2:73907344-73907642	GM12878	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73907420-73907570	GM12875	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73901987-73902164	HUVEC	blood vessel:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73929634-73929684	IMR90	lung:	fetal
2	chr2:73928500-73928550	GM06990	blood:	n/a
3	chr2:73929634-73929684	IMR90	lung:	fetal
4	chr2:73928500-73928550	GM06990	blood:	n/a
5	chr2:73907327-73907377	HEK293	kidney:	embryo
6	chr2:73928348-73928398	HRPEpiC	eye:	n/a
7	chr2:73929765-73929815	GM12891	blood:	n/a
8	chr2:73927710-73927760	SK-N-MC	brain:	n/a
9	chr2:73929634-73929684	MCF-7	breast:	n/a
10	chr2:73928492-73928542	SAEC	small airway:	n/a
11	chr2:73907327-73907377	Caco-2	colon:	n/a
12	chr2:73928492-73928542	CMK	blood:	n/a
13	chr2:73928348-73928398	GM12878	blood:	n/a
14	chr2:73927710-73927760	AG04449	skin:	fetal
15	chr2:73929892-73929942	PANC-1	pancreas:	n/a
16	chr2:73928500-73928550	HL-60	blood:	n/a
17	chr2:73929634-73929684	HCM	heart:	n/a
18	chr2:73927710-73927760	IMR90	lung:	fetal
19	chr2:73929765-73929815	SK-N-MC	brain:	n/a
20	chr2:73928492-73928542	NT2-D1	testis:	n/a
21	chr2:73928348-73928398	CMK	blood:	n/a
22	chr2:73907327-73907377	NB4	blood:	n/a
23	chr2:73907327-73907377	H1-hESC	embryonic stem cell:	embryo
24	chr2:73907327-73907377	Hepatocyte	liver:	n/a
25	chr2:73928500-73928550	NB4	blood:	n/a
26	chr2:73907327-73907377	A549	lung:	n/a
27	chr2:73928500-73928550	PrEC	prostate:	n/a
28	chr2:73929892-73929942	GM12892	blood:	n/a
29	chr2:73928348-73928398	SAEC	small airway:	n/a
30	chr2:73929634-73929684	PrEC	prostate:	n/a
31	chr2:73929634-73929684	ovcar-3	ovarian:	n/a
32	chr2:73928348-73928398	HRCEpiC	kidney:	n/a
33	chr2:73928500-73928550	AG04449	skin:	fetal
34	chr2:73929892-73929942	NHDF-neo	bronchial:	n/a
35	chr2:73928492-73928542	HCPEpiC	choroid plexus:	n/a
36	chr2:73929765-73929815	ECC-1	luminal epithelium:	n/a
37	chr2:73928348-73928398	MCF-7	breast:	n/a
38	chr2:73928348-73928398	HAEpiC	amniotic membrane:	n/a
39	chr2:73907327-73907377	SAEC	small airway:	n/a
40	chr2:73929634-73929684	CMK	blood:	n/a
41	chr2:73929892-73929942	PFSK-1	brain:	n/a
42	chr2:73927710-73927760	U87	brain:	n/a
43	chr2:73928492-73928542	H1-hESC	embryonic stem cell:	embryo
44	chr2:73928492-73928542	Hela-S3	cervix:	n/a
45	chr2:73929765-73929815	SK-N-SH_RA	brain:	n/a
46	chr2:73929892-73929942	SKMC	muscle:	n/a
47	chr2:73907327-73907377	IMR90	lung:	fetal
48	chr2:73907327-73907377	NHDF-neo	bronchial:	n/a
49	chr2:73927710-73927760	HepG2	liver:	n/a
50	chr2:73928348-73928398	NHDF-neo	bronchial:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73932554..73934998-chr2:74005796..74007372,2	MCF-7	breast:
2	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
3	chr2:73928399..73931050-chr2:73932225..73934947,2	K562	blood:
4	chr2:73943613..73945709-chr2:73953816..73955383,2	MCF-7	breast:
5	chr2:73945415..73947505-chr2:73953398..73955264,2	K562	blood:
6	chr2:73954066..73956165-chr2:73960513..73963434,2	MCF-7	breast:
7	chr2:73940417..73941921-chr2:73955171..73957279,2	MCF-7	breast:
8	chr2:73954918..73956793-chr2:73957164..73959420,2	MCF-7	breast:
9	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
10	chr2:73943613..73945709-chr2:73953816..73955383,2	MCF-7	breast:
11	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
12	chr2:73934847..73936533-chr2:73939356..73942331,2	K562	blood:
13	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
14	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
15	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
16	chr15:68480911..68481491-chr2:73955390..73956181,2	Hela-S3	cervix:
17	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
18	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
19	chr2:73934784..73936668-chr2:73963156..73965791,2	K562	blood:
20	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
21	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
22	chr2:73940417..73941921-chr2:73955171..73957279,2	MCF-7	breast:
23	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
24	chr2:73945415..73947505-chr2:73953398..73955264,2	K562	blood:
25	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
26	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
27	chr2:73927692..73931050-chr2:73931884..73934947,3	K562	blood:
28	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
29	chr2:73954874..73956746-chr2:74424567..74426478,2	MCF-7	breast:
30	chr2:73934847..73936533-chr2:73939356..73942331,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
2	lnc-C2orf78-1	chr2:73927556-73928129	ENSG00000251346
3	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
4	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
5	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
6	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
7	lnc-C2orf78-1	chr2:73933639-73934687	ENSG00000251346
8	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683

No data

Variant related genes	Relation type
ALMS1P	TF binding region
ENSG00000204872	TF binding region
ALMS1P	CpG island
ENSG00000204872	CpG island
ENSG00000144048	chromatin interactions
ENSG00000163016	chromatin interactions
ENSG00000144034	chromatin interactions
ENSG00000204872	chromatin interactions
ENSG00000144035	chromatin interactions
ENSG00000065911	chromatin interactions
UBE2I	miRNA target sites

Extended variants
information (count: 2645 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2645 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116760472	chr2:73891106-73891107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534517493	chr2:73891177-73891178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552601656	chr2:73891184-73891185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574236961	chr2:73891188-73891189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557364754	chr2:73896225-73896226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149182306	chr2:73896227-73896228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546405260	chr2:73896265-73896266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570409007	chr2:73896281-73896282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564699560	chr2:73896313-73896314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373942294	chr2:73896348-73896349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187938998	chr2:73896354-73896355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540700181	chr2:73896387-73896388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562221095	chr2:73896418-73896419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367688687	chr2:73896428-73896429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529226773	chr2:73896440-73896441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551001532	chr2:73896444-73896445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569833875	chr2:73896450-73896451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191203223	chr2:73896457-73896458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182472785	chr2:73896502-73896503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570277940	chr2:73896522-73896523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534515556	chr2:73896550-73896551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552601257	chr2:73896556-73896557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189182497	chr2:73896564-73896565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6546870	chr2:73896603-73896604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs143345362	chr2:73896630-73896631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192350289	chr2:73896631-73896632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184419848	chr2:73896670-73896671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540112167	chr2:73896724-73896725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567894717	chr2:73896764-73896765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376688107	chr2:73896765-73896766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187220081	chr2:73896769-73896770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535302701	chr2:73896812-73896813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540832817	chr2:73896830-73896831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191734793	chr2:73896887-73896888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116083343	chr2:73896915-73896916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544256944	chr2:73896927-73896928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562872393	chr2:73896936-73896937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148207145	chr2:73896949-73896950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35607349	chr2:73896950-73896951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185056678	chr2:73896957-73896958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564039370	chr2:73896983-73896984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189560772	chr2:73897014-73897015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181009856	chr2:73897026-73897027	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546428871	chr2:73897036-73897037	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568046284	chr2:73897038-73897039	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535567640	chr2:73897052-73897053	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550426913	chr2:73897070-73897071	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs568803781	chr2:73897079-73897080	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs539452817	chr2:73897083-73897084	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs572055992	chr2:73897103-73897104	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73890800-73891200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:73896200-73905200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:73896800-73897800	Enhancers	HepG2	liver
4	chr2:73897000-73897200	Enhancers	Gastric	stomach
5	chr2:73897200-73904600	Weak transcription	Gastric	stomach
6	chr2:73897400-73899600	Weak transcription	Fetal Brain Female	brain
7	chr2:73897600-73899200	Weak transcription	Ovary	ovary
8	chr2:73898000-73898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:73898000-73899600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr2:73898000-73899800	Weak transcription	Brain Angular Gyrus	brain
11	chr2:73898200-73899800	Weak transcription	Liver	Liver
12	chr2:73898200-73899800	Weak transcription	Brain Anterior Caudate	brain
13	chr2:73898400-73900000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr2:73898600-73903600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:73898800-73900200	Weak transcription	Pancreas	Pancrea
16	chr2:73898800-73901200	Weak transcription	Brain Substantia Nigra	brain
17	chr2:73899200-73901400	Weak transcription	Brain Hippocampus Middle	brain
18	chr2:73899200-73901600	Strong transcription	Ovary	ovary
19	chr2:73899200-73902200	Weak transcription	Fetal Brain Male	brain
20	chr2:73899400-73902000	Weak transcription	Aorta	Aorta
21	chr2:73899400-73902800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr2:73899600-73901200	Strong transcription	Fetal Brain Female	brain
23	chr2:73899600-73901400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:73899600-73902000	Weak transcription	Fetal Lung	lung
25	chr2:73899800-73900600	Strong transcription	Liver	Liver
26	chr2:73899800-73901400	Strong transcription	Brain Angular Gyrus	brain
27	chr2:73899800-73902200	Strong transcription	Brain Anterior Caudate	brain
28	chr2:73900000-73900600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:73900200-73900600	Strong transcription	Pancreas	Pancrea
30	chr2:73900600-73912800	Weak transcription	Liver	Liver
31	chr2:73900600-73913000	Weak transcription	Pancreas	Pancrea
32	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr2:73901200-73903400	Weak transcription	Fetal Brain Female	brain
34	chr2:73901400-73905200	Weak transcription	Brain Angular Gyrus	brain
35	chr2:73901400-73913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:73901600-73911400	Weak transcription	Ovary	ovary
37	chr2:73901800-73902400	Enhancers	GM12878-XiMat	blood
38	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain
39	chr2:73905200-73905600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:73906200-73907000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr2:73906800-73909600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:73907000-73907400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr2:73907000-73907400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr2:73907200-73907400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:73907200-73907400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:73907200-73907400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:73911400-73911600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr2:73911400-73911800	Enhancers	Ovary	ovary
49	chr2:73911800-73912800	Weak transcription	Ovary	ovary
50	chr2:73911800-73913000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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