Variant report

Variant	esv2762675
Chromosome Location	chr2:73875799-73928886
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	chr2:73907394-73907641	K562	blood:	n/a	n/a
2	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
3	ATF1	chr2:73928292-73928546	K562	blood:	n/a	n/a
4	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
5	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
6	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
8	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
9	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
10	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
12	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
14	BHLHE40	chr2:73928154-73928613	K562	blood:	n/a	n/a
15	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
16	CBX3	chr2:73928047-73928946	K562	blood:	n/a	n/a
17	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
18	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
19	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
20	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
22	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
23	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
24	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
26	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
27	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
29	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
30	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
31	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
32	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
34	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
35	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
37	CTCF	chr2:73912160-73912310	BJ	skin:	n/a	n/a
38	CTCF	chr2:73907440-73907590	GM12871	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
39	CTCF	chr2:73912176-73912322	LNCaP	prostate:	n/a	n/a
40	CTCF	chr2:73917940-73918090	HEK293	kidney:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
41	CTCF	chr2:73907440-73907590	AG04449	skin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
42	CTCF	chr2:73912260-73912410	HRE	kidney:	n/a	n/a
43	CTCF	chr2:73917940-73918090	HepG2	liver:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
44	CTCF	chr2:73907440-73907590	RPTEC	kidney:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
45	CTCF	chr2:73917869-73918137	GM10266	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
46	CTCF	chr2:73912160-73912310	GM12878	blood:	n/a	n/a
47	CTCF	chr2:73917904-73918091	GM12891	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
48	CTCF	chr2:73907440-73907590	HRPEpiC	eye:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73917940-73918090	HL-60	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
50	CTCF	chr2:73917940-73918090	AG09309	skin:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73927710-73927760	Hela-S3	cervix:	n/a
2	chr2:73928492-73928542	AG09309	skin:	n/a
3	chr2:73927710-73927760	LNCaP	prostate:	n/a
4	chr2:73907327-73907377	HCT-116	colon:	n/a
5	chr2:73907327-73907377	BE2_C	brain:	n/a
6	chr2:73907327-73907377	ECC-1	luminal epithelium:	n/a
7	chr2:73928492-73928542	HCPEpiC	choroid plexus:	n/a
8	chr2:73928492-73928542	AoSMC	blood vessel:	n/a
9	chr2:73928500-73928550	AG10803	skin:	n/a
10	chr2:73928492-73928542	SAEC	small airway:	n/a
11	chr2:73927710-73927760	HEEpiC	esophagus:	n/a
12	chr2:73907327-73907377	HCM	heart:	n/a
13	chr2:73907327-73907377	HIPEpiC	eye:	n/a
14	chr2:73928348-73928398	HCF	heart:	n/a
15	chr2:73928348-73928398	AG04450	lung:	fetal
16	chr2:73928348-73928398	PFSK-1	brain:	n/a
17	chr2:73907327-73907377	NHDF-neo	bronchial:	n/a
18	chr2:73928500-73928550	NB4	blood:	n/a
19	chr2:73928492-73928542	NB4	blood:	n/a
20	chr2:73928348-73928398	HRCEpiC	kidney:	n/a
21	chr2:73928348-73928398	MCF10A-Er-Src	breast:	n/a
22	chr2:73928500-73928550	AG04449	skin:	fetal
23	chr2:73928500-73928550	ProgFib	skin:	n/a
24	chr2:73928492-73928542	AG04450	lung:	fetal
25	chr2:73928500-73928550	Caco-2	colon:	n/a
26	chr2:73928348-73928398	HMEC	breast:	n/a
27	chr2:73928492-73928542	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:73928492-73928542	ovcar-3	ovarian:	n/a
29	chr2:73928348-73928398	LNCaP	prostate:	n/a
30	chr2:73907327-73907377	HEEpiC	esophagus:	n/a
31	chr2:73928348-73928398	HCM	heart:	n/a
32	chr2:73928500-73928550	AoSMC	blood vessel:	n/a
33	chr2:73928348-73928398	ProgFib	skin:	n/a
34	chr2:73928348-73928398	BE2_C	brain:	n/a
35	chr2:73927710-73927760	AG09319	gingival:	n/a
36	chr2:73927710-73927760	SK-N-MC	brain:	n/a
37	chr2:73928500-73928550	HNPCEpiC	eye:	n/a
38	chr2:73927710-73927760	K562	blood:	n/a
39	chr2:73907327-73907377	T-47D	breast:	n/a
40	chr2:73907327-73907377	AG10803	skin:	n/a
41	chr2:73928492-73928542	PFSK-1	brain:	n/a
42	chr2:73928500-73928550	HRCEpiC	kidney:	n/a
43	chr2:73928500-73928550	MCF-7	breast:	n/a
44	chr2:73928500-73928550	BE2_C	brain:	n/a
45	chr2:73928348-73928398	PrEC	prostate:	n/a
46	chr2:73927710-73927760	MCF-7	breast:	n/a
47	chr2:73928492-73928542	MCF10A-Er-Src	breast:	n/a
48	chr2:73907327-73907377	GM12892	blood:	n/a
49	chr2:73928492-73928542	Jurkat	blood:	n/a
50	chr2:73928348-73928398	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
2	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
3	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
4	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
5	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
6	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
7	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
8	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
9	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
10	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
11	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
12	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
13	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
14	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
15	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:

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

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

Extended variants
information (count: 1853 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1853 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553403786	chr2:73875820-73875821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554931299	chr2:73875898-73875899	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200373804	chr2:73875908-73875909	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576684801	chr2:73875914-73875915	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12478871	chr2:73875920-73875921	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549261754	chr2:73875932-73875933	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558772931	chr2:73875972-73875973	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576919690	chr2:73876026-73876027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13431529	chr2:73876041-73876042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs559301898	chr2:73876053-73876054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545259046	chr2:73876057-73876058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183996507	chr2:73876059-73876060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560982901	chr2:73876110-73876111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs57463279	chr2:73876119-73876120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs549995697	chr2:73876141-73876142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115448402	chr2:73876190-73876191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141819562	chr2:73876229-73876230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368673022	chr2:73876297-73876298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547542899	chr2:73876313-73876314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565788348	chr2:73876333-73876334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187117212	chr2:73876351-73876352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554554333	chr2:73876362-73876363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11884059	chr2:73876384-73876385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs72913485	chr2:73876400-73876401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558713650	chr2:73876434-73876435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577054255	chr2:73876452-73876453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541251256	chr2:73876493-73876494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575771255	chr2:73876495-73876496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574884937	chr2:73876574-73876575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541809621	chr2:73876621-73876622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114574662	chr2:73876623-73876624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576248322	chr2:73876678-73876679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140758853	chr2:73876704-73876705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372197469	chr2:73876723-73876724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370417025	chr2:73876753-73876754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565050077	chr2:73876758-73876759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191614966	chr2:73876795-73876796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547623034	chr2:73876808-73876809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184243422	chr2:73876828-73876829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111833974	chr2:73876845-73876846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35158565	chr2:73876884-73876885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573204445	chr2:73876894-73876895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547867768	chr2:73876905-73876906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569670022	chr2:73876933-73876934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536322556	chr2:73876955-73876956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72811973	chr2:73876966-73876967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs570827838	chr2:73876992-73876993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534846430	chr2:73877007-73877008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553533414	chr2:73877012-73877013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201103371	chr2:73877018-73877019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73868600-73877000	Weak transcription	Gastric	stomach
2	chr2:73871200-73878800	Weak transcription	Liver	Liver
3	chr2:73874600-73876000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:73876000-73880800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:73876200-73876400	Enhancers	Fetal Lung	lung
6	chr2:73876400-73877800	Weak transcription	Fetal Lung	lung
7	chr2:73877800-73878600	Enhancers	Fetal Lung	lung
8	chr2:73878200-73878800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr2:73878200-73879200	Enhancers	GM12878-XiMat	blood
10	chr2:73878800-73880000	Enhancers	Liver	Liver
11	chr2:73879200-73881600	Weak transcription	GM12878-XiMat	blood
12	chr2:73881600-73882000	Enhancers	GM12878-XiMat	blood
13	chr2:73890800-73891200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:73896200-73905200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:73896800-73897800	Enhancers	HepG2	liver
16	chr2:73897000-73897200	Enhancers	Gastric	stomach
17	chr2:73897200-73904600	Weak transcription	Gastric	stomach
18	chr2:73897400-73899600	Weak transcription	Fetal Brain Female	brain
19	chr2:73897600-73899200	Weak transcription	Ovary	ovary
20	chr2:73898000-73898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:73898000-73899600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:73898000-73899800	Weak transcription	Brain Angular Gyrus	brain
23	chr2:73898200-73899800	Weak transcription	Liver	Liver
24	chr2:73898200-73899800	Weak transcription	Brain Anterior Caudate	brain
25	chr2:73898400-73900000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:73898600-73903600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:73898800-73900200	Weak transcription	Pancreas	Pancrea
28	chr2:73898800-73901200	Weak transcription	Brain Substantia Nigra	brain
29	chr2:73899200-73901400	Weak transcription	Brain Hippocampus Middle	brain
30	chr2:73899200-73901600	Strong transcription	Ovary	ovary
31	chr2:73899200-73902200	Weak transcription	Fetal Brain Male	brain
32	chr2:73899400-73902000	Weak transcription	Aorta	Aorta
33	chr2:73899400-73902800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:73899600-73901200	Strong transcription	Fetal Brain Female	brain
35	chr2:73899600-73901400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:73899600-73902000	Weak transcription	Fetal Lung	lung
37	chr2:73899800-73900600	Strong transcription	Liver	Liver
38	chr2:73899800-73901400	Strong transcription	Brain Angular Gyrus	brain
39	chr2:73899800-73902200	Strong transcription	Brain Anterior Caudate	brain
40	chr2:73900000-73900600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr2:73900200-73900600	Strong transcription	Pancreas	Pancrea
42	chr2:73900600-73912800	Weak transcription	Liver	Liver
43	chr2:73900600-73913000	Weak transcription	Pancreas	Pancrea
44	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr2:73901200-73903400	Weak transcription	Fetal Brain Female	brain
46	chr2:73901400-73905200	Weak transcription	Brain Angular Gyrus	brain
47	chr2:73901400-73913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:73901600-73911400	Weak transcription	Ovary	ovary
49	chr2:73901800-73902400	Enhancers	GM12878-XiMat	blood
50	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain

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