Variant report

Variant	nsv874271
Chromosome Location	chr2:73847024-73907696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:981)
CpG islands
(count:1099)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:981 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
4	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73857942-73858125	HepG2	liver:	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	chr2:73857107-73857303	K562	blood:	n/a	n/a
9	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
11	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
12	BATF	chr2:73851278-73851536	GM12878	blood:	n/a	chr2:73851419-73851430
13	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
14	BATF	chr2:73851315-73851489	GM12878	blood:	n/a	chr2:73851419-73851430
15	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
17	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
18	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
19	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
21	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
22	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
25	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
27	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
29	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
31	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
33	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
35	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
40	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
41	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
42	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
43	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
44	CTCF	chr2:73874804-73875161	K562	blood:	n/a	n/a
45	CTCF	chr2:73847040-73847190	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr2:73857848-73858141	HepG2	liver:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
47	CTCF	chr2:73851829-73852065	Medullo	brain:	n/a	n/a
48	CTCF	chr2:73907391-73907621	ProgFib	skin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73847180-73847330	WERI-Rb-1	eye:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271
50	CTCF	chr2:73847160-73847310	BJ	skin:	n/a	chr2:73847256-73847269 chr2:73847255-73847276 chr2:73847254-73847270 chr2:73847256-73847265 chr2:73847253-73847271

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73868919-73868969	IMR90	lung:	fetal
2	chr2:73868919-73868969	IMR90	lung:	fetal
3	chr2:73871942-73871992	MCF-7	breast:	n/a
4	chr2:73870294-73870344	T-47D	breast:	n/a
5	chr2:73907327-73907377	NB4	blood:	n/a
6	chr2:73868917-73868967	HUVEC	blood vessel:	n/a
7	chr2:73870294-73870344	HNPCEpiC	eye:	n/a
8	chr2:73871230-73871280	H1-hESC	embryonic stem cell:	embryo
9	chr2:73867196-73867246	K562	blood:	n/a
10	chr2:73907327-73907377	AG09309	skin:	n/a
11	chr2:73907327-73907377	ECC-1	luminal epithelium:	n/a
12	chr2:73869666-73869716	HMEC	breast:	n/a
13	chr2:73870294-73870344	RPTEC	kidney:	n/a
14	chr2:73868736-73868786	HCM	heart:	n/a
15	chr2:73871230-73871280	BJ	skin:	n/a
16	chr2:73870105-73870155	PANC-1	pancreas:	n/a
17	chr2:73869666-73869716	GM12891	blood:	n/a
18	chr2:73871915-73871965	MCF-7	breast:	n/a
19	chr2:73871782-73871832	HCF	heart:	n/a
20	chr2:73871782-73871832	HAEpiC	amniotic membrane:	n/a
21	chr2:73871855-73871905	T-47D	breast:	n/a
22	chr2:73869516-73869566	PrEC	prostate:	n/a
23	chr2:73868917-73868967	AG10803	skin:	n/a
24	chr2:73868917-73868967	HEK293	kidney:	embryo
25	chr2:73871309-73871359	RPTEC	kidney:	n/a
26	chr2:73871782-73871832	AoSMC	blood vessel:	n/a
27	chr2:73869966-73870016	SK-N-SH_RA	brain:	n/a
28	chr2:73869666-73869716	PrEC	prostate:	n/a
29	chr2:73868917-73868967	A549	lung:	n/a
30	chr2:73869966-73870016	HCPEpiC	choroid plexus:	n/a
31	chr2:73869516-73869566	BE2_C	brain:	n/a
32	chr2:73871309-73871359	MCF-7	breast:	n/a
33	chr2:73867196-73867246	CMK	blood:	n/a
34	chr2:73871849-73871899	AG09319	gingival:	n/a
35	chr2:73868736-73868786	HRPEpiC	eye:	n/a
36	chr2:73871309-73871359	PANC-1	pancreas:	n/a
37	chr2:73870653-73870703	Hela-S3	cervix:	n/a
38	chr2:73869666-73869716	HNPCEpiC	eye:	n/a
39	chr2:73868919-73868969	HIPEpiC	eye:	n/a
40	chr2:73871782-73871832	T-47D	breast:	n/a
41	chr2:73868736-73868786	GM19239	blood:	n/a
42	chr2:73868919-73868969	Hela-S3	cervix:	n/a
43	chr2:73871855-73871905	AG09319	gingival:	n/a
44	chr2:73871309-73871359	ovcar-3	ovarian:	n/a
45	chr2:73870653-73870703	Jurkat	blood:	n/a
46	chr2:73869966-73870016	BJ	skin:	n/a
47	chr2:73871849-73871899	IMR90	lung:	fetal
48	chr2:73871849-73871899	AG04449	skin:	fetal
49	chr2:73869666-73869716	U87	brain:	n/a
50	chr2:73870294-73870344	PFSK-1	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73839411..73842027-chr2:73845184..73847412,3	MCF-7	breast:
2	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
3	chr2:73842508..73845608-chr2:73846002..73848469,3	K562	blood:
4	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
5	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
6	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
7	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
8	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
9	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
10	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
11	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
12	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
13	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
14	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
15	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
16	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
17	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
18	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
19	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
20	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
21	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625
2	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
3	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
4	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
5	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
6	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
7	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683

No data

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000204872	chromatin interactions
ENSG00000144048	chromatin interactions

Extended variants
information (count: 2233 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2233 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2015477	chr2:73847024-73847025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs55793240	chr2:73847027-73847028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs543695875	chr2:73847031-73847032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558575462	chr2:73847041-73847042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145508145	chr2:73847068-73847069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540886740	chr2:73847085-73847086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559373308	chr2:73847115-73847116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62149805	chr2:73847139-73847140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185523059	chr2:73847173-73847174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145349691	chr2:73847175-73847176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530568529	chr2:73847213-73847214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552790094	chr2:73847214-73847215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs55903239	chr2:73847216-73847217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528657817	chr2:73847226-73847227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs59830889	chr2:73847228-73847229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6726694	chr2:73847230-73847231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs55745821	chr2:73847246-73847247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs56131703	chr2:73847260-73847261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs568862516	chr2:73847284-73847285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531658779	chr2:73847304-73847305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374161528	chr2:73847319-73847320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6755712	chr2:73847335-73847336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577086654	chr2:73847358-73847359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541346952	chr2:73847359-73847360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553189646	chr2:73847368-73847369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562151929	chr2:73847370-73847371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574727858	chr2:73847392-73847393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6755612	chr2:73847400-73847401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs6726975	chr2:73847403-73847404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182181856	chr2:73847411-73847412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142107456	chr2:73847412-73847413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13387318	chr2:73847413-73847414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528763974	chr2:73847426-73847427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190167029	chr2:73847427-73847428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34884351	chr2:73847453-73847454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529446070	chr2:73847478-73847479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78355123	chr2:73847502-73847503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569028880	chr2:73847522-73847523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35967215	chr2:73847523-73847524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538831366	chr2:73847546-73847547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181097329	chr2:73847550-73847551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114788174	chr2:73847561-73847562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554052792	chr2:73847579-73847580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566894635	chr2:73847582-73847583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534603804	chr2:73847584-73847585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185094126	chr2:73847585-73847586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574638415	chr2:73847596-73847597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189563680	chr2:73847601-73847602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182543105	chr2:73847609-73847610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62149807	chr2:73847658-73847659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73830600-73847600	Weak transcription	Spleen	Spleen
2	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:73836400-73852600	Weak transcription	Ovary	ovary
4	chr2:73838400-73852600	Weak transcription	Right Ventricle	heart
5	chr2:73838600-73847400	Weak transcription	Brain Angular Gyrus	brain
6	chr2:73838600-73852600	Weak transcription	Pancreas	Pancrea
7	chr2:73838800-73849600	Weak transcription	Brain Germinal Matrix	brain
8	chr2:73842600-73852600	Weak transcription	Left Ventricle	heart
9	chr2:73844000-73854800	Weak transcription	Fetal Brain Female	brain
10	chr2:73844200-73848800	Weak transcription	Aorta	Aorta
11	chr2:73850000-73850200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr2:73850200-73852400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:73850800-73851400	Enhancers	GM12878-XiMat	blood
14	chr2:73851400-73853000	Weak transcription	GM12878-XiMat	blood
15	chr2:73852000-73852600	Enhancers	HepG2	liver
16	chr2:73852400-73852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:73852400-73854000	Enhancers	Liver	Liver
18	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr2:73852600-73852800	Enhancers	Fetal Intestine Large	intestine
20	chr2:73852600-73852800	Enhancers	Left Ventricle	heart
21	chr2:73852600-73852800	Flanking Active TSS	HepG2	liver
22	chr2:73852600-73853000	Enhancers	Colonic Mucosa	Colon
23	chr2:73852600-73853200	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr2:73852600-73853200	Enhancers	Duodenum Mucosa	Duodenum
25	chr2:73852600-73853200	Enhancers	Pancreas	Pancrea
26	chr2:73852600-73853200	Enhancers	Right Ventricle	heart
27	chr2:73852600-73853800	Enhancers	Ovary	ovary
28	chr2:73852600-73854000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:73852600-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:73852600-73854400	Enhancers	Primary hematopoietic stem cells	blood
31	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr2:73852800-73853000	Enhancers	HepG2	liver
33	chr2:73852800-73853200	Enhancers	A549	lung
34	chr2:73852800-73853200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr2:73853000-73853200	Flanking Active TSS	HepG2	liver
36	chr2:73853000-73853400	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr2:73853000-73854000	Enhancers	GM12878-XiMat	blood
38	chr2:73853200-73853600	Enhancers	HepG2	liver
39	chr2:73853400-73853600	Enhancers	Fetal Intestine Large	intestine
40	chr2:73853800-73854000	Weak transcription	Ovary	ovary
41	chr2:73854000-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:73854000-73858000	Weak transcription	Liver	Liver
43	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
45	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
46	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
47	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
48	chr2:73857000-73857200	Active TSS	NHLF	lung
49	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
50	chr2:73857000-73857400	Active TSS	HSMM	muscle

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