Variant report

Variant	esv6387
Chromosome Location	chr6:58775945-58777262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:87)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:59487756..59489295-chr6:58776969..58779008,2	MCF-7	breast:
2	chr17:57928094..57930742-chr6:58776120..58778676,4	MCF-7	breast:
3	chr6:27776232..27779951-chr6:58776955..58780402,3	MCF-7	breast:
4	chr12:117585721..117587663-chr6:58775712..58777632,2	MCF-7	breast:
5	chr15:50229689..50230313-chr6:58776456..58777229,2	MCF-7	breast:
6	chr6:58776953..58777924-chr9:126446426..126447140,2	MCF-7	breast:
7	chr17:57914586..57918340-chr6:58776843..58780440,4	MCF-7	breast:
8	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
9	chr17:56707689..56709464-chr6:58776179..58779153,2	MCF-7	breast:
10	chr6:58777104..58777807-chr8:123404144..123404872,2	MCF-7	breast:
11	chr2:109819769..109820303-chr6:58776869..58777442,2	MCF-7	breast:
12	chr17:57920187..57922882-chr6:58774753..58776582,2	MCF-7	breast:
13	chr12:38031911..38033432-chr6:58776341..58779018,2	MCF-7	breast:
14	chr4:26787771..26789874-chr6:58775360..58778093,2	MCF-7	breast:
15	chr20:46012525..46013472-chr6:58776071..58776784,2	MCF-7	breast:
16	chr6:58776722..58778356-chr8:48323824..48325324,2	MCF-7	breast:
17	chr20:52815826..52816411-chr6:58777180..58778164,2	MCF-7	breast:
18	chr17:30334360..30334893-chr6:58777200..58777864,2	Hela-S3	cervix:
19	chr6:30581365..30583375-chr6:58776545..58779152,2	MCF-7	breast:
20	chr6:58776858..58779077-chr6:61908295..61909815,2	MCF-7	breast:
21	chr3:90451070..90451591-chr6:58777113..58777718,3	MCF-7	breast:
22	chr6:58776666..58779159-chr8:125462787..125464378,2	MCF-7	breast:
23	chr1:216349276..216351630-chr6:58776732..58778763,2	MCF-7	breast:
24	chr20:36661511..36663112-chr6:58773928..58776889,2	K562	blood:
25	chr13:111364963..111367929-chr6:58777252..58779728,2	MCF-7	breast:
26	chr20:52560026..52560620-chr6:58777219..58777738,2	MCF-7	breast:
27	chr6:58776120..58778273-chr8:145699925..145701982,2	MCF-7	breast:
28	chr14:77757334..77757890-chr6:58776828..58777663,2	MCF-7	breast:
29	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
30	chr3:63980131..63982580-chr6:58776275..58779243,2	MCF-7	breast:
31	chr20:52327864..52329489-chr6:58775870..58778258,2	MCF-7	breast:
32	chr12:80435495..80437852-chr6:58775102..58777367,2	MCF-7	breast:
33	chr2:219259923..219262856-chr6:58776591..58778942,2	MCF-7	breast:
34	chr12:38031932..38033432-chr6:58775709..58777615,2	MCF-7	breast:
35	chr20:45984506..45987023-chr6:58776231..58780015,3	MCF-7	breast:
36	chr21:9826269..9827015-chr6:58776389..58777037,2	MCF-7	breast:
37	chr20:52424572..52427398-chr6:58777006..58778744,2	MCF-7	breast:
38	chr22:21356184..21359058-chr6:58776120..58778924,2	MCF-7	breast:
39	chr10:74031778..74033740-chr6:58774757..58776794,2	MCF-7	breast:
40	chr17:56707619..56709303-chr6:58776177..58777680,2	MCF-7	breast:
41	chr11:66445363..66446008-chr6:58776703..58777356,2	MCF-7	breast:
42	chr12:38032931..38033431-chr6:58776879..58777388,2	MCF-7	breast:
43	chr1:117112641..117113268-chr6:58775753..58776519,2	MCF-7	breast:
44	chr5:157496471..157496971-chr6:58776705..58777406,2	MCF-7	breast:
45	chr14:19022553..19024053-chr6:58774785..58777168,2	MCF-7	breast:
46	chr1:201243876..201245779-chr6:58775647..58777227,2	MCF-7	breast:
47	chr11:58678524..58679504-chr6:58776958..58777672,3	MCF-7	breast:
48	chr3:195577616..195578367-chr6:58777226..58778078,2	MCF-7	breast:
49	chr6:58773141..58775009-chr6:58776566..58778429,2	MCF-7	breast:
50	chr16:85495639..85498852-chr6:58775657..58778770,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000175866	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000101413	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000159202	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000248278	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000226137	chromatin interactions
ENSG00000101407	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000104524	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000185158	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000160973	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000184436	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000237080	chromatin interactions
ENSG00000141367	chromatin interactions
ENSG00000048392	chromatin interactions

Extended variants
information (count: 865 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546243424	chr6:58775945-58775946	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs201553949	chr6:58775953-58775954	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs565154214	chr6:58775956-58775957	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs577049670	chr6:58775957-58775958	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs541348005	chr6:58775961-58775962	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs559283201	chr6:58775962-58775963	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs78674415	chr6:58775963-58775964	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs148111096	chr6:58775965-58775966	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs547838384	chr6:58775969-58775970	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs9500415	chr6:58775970-58775971	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs530395561	chr6:58775971-58775972	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs75008291	chr6:58775975-58775976	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs551901245	chr6:58775976-58775977	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs79220608	chr6:58775978-58775979	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs142543655	chr6:58775980-58775981	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs570460626	chr6:58775981-58775982	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs140478125	chr6:58775989-58775990	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs528757960	chr6:58775993-58775994	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs77183951	chr6:58775995-58775996	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs149140861	chr6:58775998-58775999	ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs75729024	chr6:58776000-58776001	ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs112332512	chr6:58776002-58776003	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs12173619	chr6:58776003-58776004	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs149463867	chr6:58776004-58776005	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs113062862	chr6:58776006-58776007	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs142648035	chr6:58776011-58776012	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs536059948	chr6:58776014-58776015	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs28795091	chr6:58776015-58776016	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs557464989	chr6:58776016-58776017	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs575586705	chr6:58776017-58776018	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs9377860	chr6:58776021-58776022	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs202059703	chr6:58776023-58776024	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs569391383	chr6:58776025-58776026	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs539958529	chr6:58776027-58776028	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs557848324	chr6:58776032-58776033	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs149515536	chr6:58776037-58776038	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs113123411	chr6:58776040-58776041	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs76134466	chr6:58776044-58776045	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs553239260	chr6:58776045-58776046	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs9391453	chr6:58776050-58776051	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs574244755	chr6:58776052-58776053	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs4928487	chr6:58776063-58776064	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs563008991	chr6:58776065-58776066	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs6938166	chr6:58776066-58776067	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs6588728	chr6:58776069-58776070	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs60132493	chr6:58776070-58776071	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs61623650	chr6:58776071-58776072	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs376461597	chr6:58776072-58776073	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs530505357	chr6:58776073-58776074	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs4602737	chr6:58776078-58776079	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58776000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:58773400-58776000	ZNF genes & repeats	NH-A	brain
3	chr6:58773400-58776200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr6:58773400-58776200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:58773400-58776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:58773400-58776400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
9	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
10	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
11	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
16	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
17	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
19	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
20	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells from cord blood	blood
21	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:58773600-58779200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
23	chr6:58773600-58779400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
24	chr6:58773600-58779400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr6:58773600-58779400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr6:58773600-58779400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr6:58773600-58779400	ZNF genes & repeats	Primary B cells from cord blood	blood
28	chr6:58773600-58779400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
29	chr6:58773600-58779400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:58773600-58779400	ZNF genes & repeats	Fetal Intestine Large	intestine
31	chr6:58774800-58776400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:58774800-58776400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:58774800-58776400	Weak transcription	Brain Germinal Matrix	brain
34	chr6:58774800-58776600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:58774800-58776600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:58774800-58776600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:58774800-58776600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr6:58774800-58776600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr6:58774800-58776600	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr6:58774800-58776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:58774800-58776600	Weak transcription	Brain Hippocampus Middle	brain
42	chr6:58774800-58776600	Weak transcription	Esophagus	oesophagus
43	chr6:58774800-58776600	Weak transcription	Fetal Brain Male	brain
44	chr6:58774800-58776600	Weak transcription	Fetal Heart	heart
45	chr6:58774800-58776600	Weak transcription	Fetal Kidney	kidney
46	chr6:58774800-58776600	Weak transcription	Placenta	Placenta
47	chr6:58774800-58776600	Weak transcription	Lung	lung
48	chr6:58774800-58776600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr6:58774800-58776600	Weak transcription	Right Atrium	heart
50	chr6:58774800-58776600	Weak transcription	Right Ventricle	heart

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