Variant report

Variant	esv2753133
Chromosome Location	chr15:45105876-45268182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1342)
CpG islands
(count:367)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45123098-45123535	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:45145528-45145856	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:45181194-45181211	K562	blood:	n/a	n/a
4	ARID3A	chr15:45125283-45125468	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:45205265-45205621	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:45112947-45113068	K562	blood:	n/a	n/a
7	ARID3A	chr15:45123189-45123508	K562	blood:	n/a	n/a
8	ARID3A	chr15:45128282-45128791	HepG2	liver:	n/a	n/a
9	ATF1	chr15:45112841-45113209	K562	blood:	n/a	n/a
10	ATF1	chr15:45123175-45123515	K562	blood:	n/a	n/a
11	ATF1	chr15:45168202-45168273	K562	blood:	n/a	n/a
12	ATF1	chr15:45182020-45182040	K562	blood:	n/a	n/a
13	ATF1	chr15:45110150-45110343	K562	blood:	n/a	n/a
14	ATF1	chr15:45145566-45145860	K562	blood:	n/a	n/a
15	ATF2	chr15:45203385-45203780	GM12878	blood:	n/a	n/a
16	ATF2	chr15:45174666-45175297	GM12878	blood:	n/a	n/a
17	ATF2	chr15:45174555-45175594	GM12878	blood:	n/a	n/a
18	ATF2	chr15:45203414-45203775	GM12878	blood:	n/a	n/a
19	BACH1	chr15:45146115-45146175	K562	blood:	n/a	n/a
20	BATF	chr15:45214951-45215126	GM12878	blood:	n/a	n/a
21	BATF	chr15:45203489-45203757	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
22	BATF	chr15:45204924-45205158	GM12878	blood:	n/a	chr15:45204943-45204952
23	BATF	chr15:45145545-45145867	GM12878	blood:	n/a	n/a
24	BATF	chr15:45131166-45131498	GM12878	blood:	n/a	n/a
25	BATF	chr15:45175615-45176106	GM12878	blood:	n/a	n/a
26	BATF	chr15:45260122-45260297	GM12878	blood:	n/a	n/a
27	BATF	chr15:45174500-45176189	GM12878	blood:	n/a	n/a
28	BATF	chr15:45191999-45192251	GM12878	blood:	n/a	n/a
29	BATF	chr15:45131114-45131510	GM12878	blood:	n/a	n/a
30	BATF	chr15:45191947-45192347	GM12878	blood:	n/a	n/a
31	BATF	chr15:45174732-45175340	GM12878	blood:	n/a	n/a
32	BATF	chr15:45203408-45203799	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
33	BCL11A	chr15:45174655-45175245	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:45175527-45176004	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:45137220-45137412	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:45175417-45176211	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:45191932-45192270	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:45203459-45203776	GM12878	blood:	n/a	chr15:45203595-45203604 chr15:45203594-45203603
39	BCL11A	chr15:45131165-45131444	GM12878	blood:	n/a	chr15:45131356-45131365
40	BCL11A	chr15:45174637-45175348	GM12878	blood:	n/a	n/a
41	BCL3	chr15:45174662-45175296	GM12878	blood:	n/a	n/a
42	BCLAF1	chr15:45173453-45173866	GM12878	blood:	n/a	n/a
43	BCLAF1	chr15:45145496-45145860	GM12878	blood:	n/a	n/a
44	BCLAF1	chr15:45174315-45175214	GM12878	blood:	n/a	n/a
45	BCLAF1	chr15:45174481-45175331	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:45111516-45111681	K562	blood:	n/a	n/a
47	BHLHE40	chr15:45145489-45145849	HepG2	liver:	n/a	n/a
48	BHLHE40	chr15:45174566-45175326	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:45128329-45128658	HepG2	liver:	n/a	chr15:45128479-45128495
50	BHLHE40	chr15:45116583-45116784	HepG2	liver:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45248463-45248513	NHBE	bronchial:	n/a
2	chr15:45248463-45248513	NHBE	bronchial:	n/a
3	chr15:45248744-45248794	Hepatocyte	liver:	n/a
4	chr15:45248878-45248928	NH-A	brain:	n/a
5	chr15:45247870-45247920	Caco-2	colon:	n/a
6	chr15:45248878-45248928	HIPEpiC	eye:	n/a
7	chr15:45248806-45248856	IMR90	lung:	fetal
8	chr15:45248932-45248982	HPAEpiC	pulmonary alveolar:	n/a
9	chr15:45248878-45248928	HEEpiC	esophagus:	n/a
10	chr15:45248463-45248513	ECC-1	luminal epithelium:	n/a
11	chr15:45248806-45248856	MCF-7	breast:	n/a
12	chr15:45248744-45248794	IMR90	lung:	fetal
13	chr15:45247870-45247920	HRCEpiC	kidney:	n/a
14	chr15:45248932-45248982	Caco-2	colon:	n/a
15	chr15:45248806-45248856	HIPEpiC	eye:	n/a
16	chr15:45248806-45248856	HNPCEpiC	eye:	n/a
17	chr15:45248744-45248794	AG09319	gingival:	n/a
18	chr15:45248806-45248856	HRPEpiC	eye:	n/a
19	chr15:45248932-45248982	PrEC	prostate:	n/a
20	chr15:45247870-45247920	PrEC	prostate:	n/a
21	chr15:45248806-45248856	ovcar-3	ovarian:	n/a
22	chr15:45248463-45248513	HCPEpiC	choroid plexus:	n/a
23	chr15:45248744-45248794	Caco-2	colon:	n/a
24	chr15:45248463-45248513	K562	blood:	n/a
25	chr15:45248878-45248928	SKMC	muscle:	n/a
26	chr15:45248878-45248928	Caco-2	colon:	n/a
27	chr15:45248463-45248513	BE2_C	brain:	n/a
28	chr15:45248463-45248513	AG09309	skin:	n/a
29	chr15:45248463-45248513	HAEpiC	amniotic membrane:	n/a
30	chr15:45248463-45248513	ovcar-3	ovarian:	n/a
31	chr15:45248806-45248856	RPTEC	kidney:	n/a
32	chr15:45248463-45248513	SK-N-MC	brain:	n/a
33	chr15:45247870-45247920	MCF-7	breast:	n/a
34	chr15:45247870-45247920	ECC-1	luminal epithelium:	n/a
35	chr15:45248744-45248794	AG10803	skin:	n/a
36	chr15:45248878-45248928	GM12891	blood:	n/a
37	chr15:45247870-45247920	HEEpiC	esophagus:	n/a
38	chr15:45247870-45247920	U87	brain:	n/a
39	chr15:45248878-45248928	NB4	blood:	n/a
40	chr15:45248878-45248928	HUVEC	blood vessel:	n/a
41	chr15:45248932-45248982	AG04450	lung:	fetal
42	chr15:45248744-45248794	A549	lung:	n/a
43	chr15:45248463-45248513	NHDF-neo	bronchial:	n/a
44	chr15:45248744-45248794	U87	brain:	n/a
45	chr15:45248744-45248794	NT2-D1	testis:	n/a
46	chr15:45247870-45247920	BE2_C	brain:	n/a
47	chr15:45248806-45248856	AG10803	skin:	n/a
48	chr15:45247870-45247920	PFSK-1	brain:	n/a
49	chr15:45247870-45247920	H1-hESC	embryonic stem cell:	embryo
50	chr15:45248463-45248513	RPTEC	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45153661..45154310-chr15:45315073..45315837,2	NB4	blood:
2	chr15:45098451..45101074-chr15:45104343..45106886,2	K562	blood:
3	chr15:45145307..45146142-chr15:45409718..45410518,2	K562	blood:
4	chr15:45003163..45005190-chr15:45225441..45227864,2	K562	blood:
5	chr15:45002455..45004685-chr15:45109842..45111861,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf43-1	chr15:45211574-45211851	NONHSAT042202
2	lnc-C15orf43-2	chr15:45174295-45174981	NONHSAT042199
3	lnc-TRIM69-1	chr15:45118738-45118965	ENSG00000259187.1
4	lnc-DUOX2-4	chr15:45262233-45263376	NONHSAT042205
5	lnc-C15orf43-1	chr15:45212156-45213018	NONHSAT042202
6	lnc-TRIM69-1	chr15:45119097-45119292	ENSG00000259187.1

No data

Variant related genes	Relation type
ENSG00000259304	TF binding region
RNU6-1108P	TF binding region
ENSG00000259479	TF binding region
RNU6-966P	TF binding region
C15orf43	TF binding region
RNU6-1332P	TF binding region
ENSG00000259231	TF binding region
ENSG00000259187	TF binding region
ENSG00000238845	TF binding region
RNU1-119P	TF binding region
ENSG00000259742	TF binding region
ENSG00000259304	CpG island
RNU6-1108P	CpG island
ENSG00000259479	CpG island
RNU6-966P	CpG island
C15orf43	CpG island
RNU6-1332P	CpG island
ENSG00000259231	CpG island
ENSG00000259187	CpG island
ENSG00000238845	CpG island
RNU1-119P	CpG island
ENSG00000259742	CpG island
ENSG00000229474	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000140263	chromatin interactions

Extended variants
information (count: 3617 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3617 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2443982	chr15:45105876-45105877	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373873914	chr15:45105923-45105924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561789771	chr15:45105944-45105945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147328453	chr15:45105960-45105961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547125599	chr15:45106015-45106016	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs560311720	chr15:45106052-45106053	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs561127222	chr15:45106080-45106081	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553883757	chr15:45106139-45106140	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs377348268	chr15:45106240-45106241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532708110	chr15:45106264-45106265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139343066	chr15:45106291-45106292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568938927	chr15:45106299-45106300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2123145	chr15:45106334-45106335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114225677	chr15:45106380-45106381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548406832	chr15:45106446-45106447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77219490	chr15:45106447-45106448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74009438	chr15:45106460-45106461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561723780	chr15:45106469-45106470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144775956	chr15:45106496-45106497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370255470	chr15:45106532-45106533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577099686	chr15:45106539-45106540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148438698	chr15:45106544-45106545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572377735	chr15:45106571-45106572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142573700	chr15:45106637-45106638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556471184	chr15:45106758-45106759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2470920	chr15:45106771-45106772	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs541769839	chr15:45106781-45106782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561632783	chr15:45106783-45106784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191720053	chr15:45106845-45106846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114210418	chr15:45106862-45106863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150523195	chr15:45106877-45106878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181860988	chr15:45106911-45106912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78393665	chr15:45106951-45106952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375366157	chr15:45106953-45106954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79115082	chr15:45106971-45106972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562804871	chr15:45106986-45106987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531616734	chr15:45106987-45106988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543599747	chr15:45106998-45106999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186425568	chr15:45107024-45107025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568358429	chr15:45107043-45107044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531897808	chr15:45107059-45107060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565093079	chr15:45107076-45107077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371524575	chr15:45107105-45107106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547893101	chr15:45107112-45107113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570684027	chr15:45107122-45107123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112140097	chr15:45107150-45107151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556507935	chr15:45107171-45107172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569886203	chr15:45107175-45107176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535382389	chr15:45107204-45107205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79970375	chr15:45107242-45107243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45094800-45111600	Weak transcription	Right Atrium	heart
2	chr15:45102000-45106200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr15:45102200-45106200	Enhancers	Fetal Intestine Large	intestine
4	chr15:45102600-45106400	Enhancers	Liver	Liver
5	chr15:45102800-45106200	Enhancers	Stomach Mucosa	stomach
6	chr15:45102800-45106200	Enhancers	Dnd41	blood
7	chr15:45104800-45106200	Enhancers	Duodenum Mucosa	Duodenum
8	chr15:45104800-45106200	Enhancers	HepG2	liver
9	chr15:45104800-45109200	Weak transcription	K562	blood
10	chr15:45104800-45111200	Weak transcription	Left Ventricle	heart
11	chr15:45104800-45111400	Weak transcription	Pancreas	Pancrea
12	chr15:45104800-45111600	Weak transcription	Gastric	stomach
13	chr15:45105000-45106800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr15:45105400-45106000	Enhancers	Fetal Heart	heart
15	chr15:45105400-45106200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr15:45105400-45106200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr15:45105800-45106000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr15:45105800-45121600	Weak transcription	Fetal Intestine Small	intestine
19	chr15:45106000-45106200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr15:45106000-45110800	Weak transcription	Fetal Heart	heart
21	chr15:45106200-45107800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr15:45106200-45109000	Weak transcription	HepG2	liver
23	chr15:45106200-45111000	Weak transcription	Stomach Mucosa	stomach
24	chr15:45106400-45107800	Weak transcription	Liver	Liver
25	chr15:45107800-45108000	Enhancers	Liver	Liver
26	chr15:45107800-45108000	Enhancers	Duodenum Mucosa	Duodenum
27	chr15:45108000-45110800	Weak transcription	Liver	Liver
28	chr15:45108800-45111600	Weak transcription	Esophagus	oesophagus
29	chr15:45109000-45109400	Enhancers	HepG2	liver
30	chr15:45109200-45110000	Enhancers	K562	blood
31	chr15:45109400-45110200	Weak transcription	HepG2	liver
32	chr15:45110000-45110400	Flanking Active TSS	K562	blood
33	chr15:45110200-45113600	Enhancers	HepG2	liver
34	chr15:45110400-45112600	Enhancers	K562	blood
35	chr15:45110800-45113400	Enhancers	Fetal Heart	heart
36	chr15:45110800-45113600	Enhancers	Liver	Liver
37	chr15:45111000-45113400	Enhancers	Stomach Mucosa	stomach
38	chr15:45111200-45112800	Enhancers	Left Ventricle	heart
39	chr15:45111400-45111600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr15:45111400-45112000	Enhancers	Right Ventricle	heart
41	chr15:45111400-45112600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr15:45111400-45112800	Enhancers	Pancreas	Pancrea
43	chr15:45111400-45113400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr15:45111600-45111800	Enhancers	Right Atrium	heart
45	chr15:45111600-45112000	Enhancers	Esophagus	oesophagus
46	chr15:45111600-45112000	Enhancers	Gastric	stomach
47	chr15:45111600-45112600	Enhancers	Lung	lung
48	chr15:45111800-45112200	Weak transcription	Right Atrium	heart
49	chr15:45112000-45123000	Weak transcription	Esophagus	oesophagus
50	chr15:45112200-45112600	Enhancers	Right Atrium	heart

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