Variant report

Variant	nsv38
Chromosome Location	chr8:126593465-126639253
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:114)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:126593642..126596532-chr8:126599701..126606279,16	MCF-7	breast:
2	chr8:126619990..126624184-chr8:126625667..126627988,3	K562	blood:
3	chr8:126584493..126586027-chr8:126604796..126607336,2	MCF-7	breast:
4	chr8:126593642..126596532-chr8:126599701..126606279,16	MCF-7	breast:
5	chr8:126601003..126603272-chr8:126603536..126606567,4	MCF-7	breast:
6	chr8:126592961..126594666-chr8:126603938..126605486,2	MCF-7	breast:
7	chr8:126635661..126638350-chr8:126643395..126645351,2	K562	blood:
8	chr8:126619990..126624184-chr8:126625667..126627988,3	K562	blood:
9	chr8:126449216..126452088-chr8:126604011..126606730,3	MCF-7	breast:
10	chr8:126610315..126613289-chr8:126653712..126655623,2	MCF-7	breast:
11	chr8:126550463..126552355-chr8:126601119..126603239,2	MCF-7	breast:
12	chr8:126620542..126623199-chr8:126642002..126644865,2	MCF-7	breast:
13	chr8:126612725..126615017-chr8:126618565..126620143,2	MCF-7	breast:
14	chr8:126634124..126636171-chr8:126637247..126639701,2	MCF-7	breast:
15	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
16	chr8:126592991..126596537-chr8:126599819..126603670,10	MCF-7	breast:
17	chr8:126441513..126444151-chr8:126635874..126638434,2	MCF-7	breast:
18	chr8:126290887..126293286-chr8:126610271..126611815,2	K562	blood:
19	chr8:126606536..126608218-chr8:126626974..126628718,2	MCF-7	breast:
20	chr8:126242654..126243238-chr8:126601971..126602543,2	MCF-7	breast:
21	chr8:126634124..126636171-chr8:126637247..126639701,2	MCF-7	breast:
22	chr8:126612687..126615177-chr8:126616929..126619166,2	MCF-7	breast:
23	chr8:126602067..126602597-chr8:126618483..126619059,2	MCF-7	breast:
24	chr8:126591683..126594528-chr8:126604953..126606548,2	K562	blood:
25	chr8:126636675..126638535-chr8:126641760..126643803,2	MCF-7	breast:
26	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
27	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
28	chr8:126445273..126447091-chr8:126638260..126639894,2	MCF-7	breast:
29	chr8:126593358..126595719-chr8:126599796..126603386,4	K562	blood:
30	chr8:126507152..126508926-chr8:126605095..126607004,2	MCF-7	breast:
31	chr8:126616447..126617973-chr8:126621582..126623418,2	MCF-7	breast:
32	chr8:126605005..126607033-chr8:126613419..126615572,2	MCF-7	breast:
33	chr8:126624246..126627028-chr8:126627335..126628862,2	MCF-7	breast:
34	chr8:126605898..126607935-chr8:126618594..126621504,4	MCF-7	breast:
35	chr8:126446451..126446990-chr8:126594852..126595545,2	MCF-7	breast:
36	chr8:126605005..126607033-chr8:126613419..126615572,2	MCF-7	breast:
37	chr8:126593622..126595846-chr8:126610575..126612204,2	MCF-7	breast:
38	chr8:126623702..126626459-chr8:126629825..126632775,2	K562	blood:
39	chr8:126602321..126604094-chr8:126616027..126618273,2	MCF-7	breast:
40	chr8:126551415..126553791-chr8:126604012..126607735,3	MCF-7	breast:
41	chr8:126455135..126457376-chr8:126604842..126607089,2	MCF-7	breast:
42	chr8:126586635..126589036-chr8:126593188..126594968,2	MCF-7	breast:
43	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
44	chr8:126555753..126558419-chr8:126632205..126633787,2	MCF-7	breast:
45	chr8:126442074..126444761-chr8:126614097..126617217,3	MCF-7	breast:
46	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
47	chr8:126606627..126608562-chr8:126611107..126612785,3	MCF-7	breast:
48	chr8:126442143..126446665-chr8:126589959..126594389,6	MCF-7	breast:
49	chr8:126589816..126592471-chr8:126605971..126608086,2	MCF-7	breast:
50	chr8:126593622..126595846-chr8:126610575..126612204,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIB1-12	chr8:126626798-126627375	NONHSAT128977
2	lnc-TRIB1-12	chr8:126625712-126626709	NONHSAT128977

No data

Variant related genes	Relation type
ENSG00000173334	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000266452	chromatin interactions
ENSG00000164961	chromatin interactions

Extended variants
information (count: 1587 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115499908	chr8:126593505-126593506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529010186	chr8:126593518-126593519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577952331	chr8:126593570-126593571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188103191	chr8:126593571-126593572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117532689	chr8:126593586-126593587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545834515	chr8:126593592-126593593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34829029	chr8:126593605-126593606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181952058	chr8:126593606-126593607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs60495766	chr8:126593613-126593614	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372280191	chr8:126593624-126593625	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528733314	chr8:126593652-126593653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186567611	chr8:126593746-126593747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375342597	chr8:126593772-126593773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191028934	chr8:126593783-126593784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139296757	chr8:126593802-126593803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371873170	chr8:126593814-126593815	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550671148	chr8:126593821-126593822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200727122	chr8:126593871-126593872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570593422	chr8:126593877-126593878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182097777	chr8:126593890-126593891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546662648	chr8:126594006-126594007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186697342	chr8:126594010-126594011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191494324	chr8:126594013-126594014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555656989	chr8:126594026-126594027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548665985	chr8:126594051-126594052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182843570	chr8:126594085-126594086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537684934	chr8:126594160-126594161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557027653	chr8:126594177-126594178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576970306	chr8:126594183-126594184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531578852	chr8:126594217-126594218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185082060	chr8:126594311-126594312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567430767	chr8:126594336-126594337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189548762	chr8:126594360-126594361	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573205432	chr8:126594368-126594369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534803593	chr8:126594383-126594384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552088232	chr8:126594396-126594397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182167983	chr8:126594399-126594400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577984343	chr8:126594423-126594424	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs111643447	chr8:126594432-126594433	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs530994004	chr8:126594481-126594482	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs551234705	chr8:126594612-126594613	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369277228	chr8:126594614-126594615	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533008872	chr8:126594623-126594624	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187935306	chr8:126594639-126594640	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556653433	chr8:126594641-126594642	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368506617	chr8:126594667-126594668	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115958368	chr8:126594698-126594699	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548994143	chr8:126594706-126594707	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140967755	chr8:126594707-126594708	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7016867	chr8:126594738-126594739	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Gastric cancer	21635755	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126587000-126594600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:126587800-126594800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:126589600-126594600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:126589800-126594400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:126592200-126594600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:126592600-126603800	Weak transcription	Pancreas	Pancrea
7	chr8:126592800-126595400	Weak transcription	Brain Substantia Nigra	brain
8	chr8:126593000-126594600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr8:126594400-126595000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:126594600-126594800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:126594600-126595000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:126594600-126595000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:126594600-126595000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:126594600-126595000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr8:126594600-126595200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:126594600-126595200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:126594800-126595200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr8:126595000-126601200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:126600000-126604200	Weak transcription	Aorta	Aorta
20	chr8:126601200-126601600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:126601600-126602000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:126602000-126603000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:126602200-126602400	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr8:126602200-126603400	Enhancers	GM12878-XiMat	blood
25	chr8:126602200-126603600	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr8:126602200-126604400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:126602200-126606600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:126602200-126608600	Enhancers	Placenta	Placenta
29	chr8:126602400-126602800	Enhancers	Primary B cells from peripheral blood	blood
30	chr8:126602400-126603000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:126602400-126606800	Enhancers	NHEK	skin
32	chr8:126602400-126607400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr8:126602600-126605400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:126602600-126606800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:126602800-126603400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:126602800-126603800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr8:126602800-126607400	Weak transcription	Primary B cells from peripheral blood	blood
38	chr8:126603000-126603400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:126603200-126604200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:126603400-126604600	Enhancers	Fetal Intestine Small	intestine
41	chr8:126603400-126605400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:126603600-126603800	Enhancers	A549	lung
43	chr8:126603600-126604000	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr8:126603600-126605200	Enhancers	HMEC	breast
45	chr8:126603800-126604600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr8:126603800-126607000	Enhancers	Esophagus	oesophagus
47	chr8:126603800-126607200	Enhancers	Pancreas	Pancrea
48	chr8:126604000-126605600	Weak transcription	A549	lung
49	chr8:126604000-126605800	Enhancers	HSMMtube	muscle
50	chr8:126604000-126606200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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