Variant report

Variant	esv8678
Chromosome Location	chr6:58775025-58778770
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:137)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:58778355..58778904-chrX:56755266..56755790,2	MCF-7	breast:
2	chr17:57930610..57932922-chr6:58777438..58780644,3	MCF-7	breast:
3	chr6:58777751..58780199-chr8:128748477..128750306,2	MCF-7	breast:
4	chr20:60877312..60877975-chr6:58777171..58777835,2	MCF-7	breast:
5	chr6:58777993..58779849-chr8:94211437..94213575,2	MCF-7	breast:
6	chr5:157496470..157497451-chr6:58776593..58777234,3	MCF-7	breast:
7	chr17:59487756..59489295-chr6:58776969..58779008,2	MCF-7	breast:
8	chr12:38031932..38033432-chr6:58775709..58777615,2	MCF-7	breast:
9	chr20:45984506..45987023-chr6:58776231..58780015,3	MCF-7	breast:
10	chr20:52424572..52427398-chr6:58777006..58778744,2	MCF-7	breast:
11	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
12	chr16:19191197..19191940-chr6:58777386..58777915,2	MCF-7	breast:
13	chr19:35488627..35490321-chr6:58777408..58779728,2	MCF-7	breast:
14	chr12:38032931..38033431-chr6:58776879..58777388,2	MCF-7	breast:
15	chr17:56707689..56709464-chr6:58776179..58779153,2	MCF-7	breast:
16	chr6:58776120..58778273-chr8:145699925..145701982,2	MCF-7	breast:
17	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
18	chr11:58678524..58679504-chr6:58776958..58777672,3	MCF-7	breast:
19	chr20:45901715..45902477-chr6:58778556..58779159,2	MCF-7	breast:
20	chr1:144533667..144534206-chr6:58778266..58778827,2	Hela-S3	cervix:
21	chr1:201243876..201245779-chr6:58775647..58777227,2	MCF-7	breast:
22	chr12:80435495..80437852-chr6:58775102..58777367,2	MCF-7	breast:
23	chr2:38304500..38306516-chr6:58776846..58778352,2	MCF-7	breast:
24	chr6:58778414..58779270-chr7:26240803..26241518,2	Hela-S3	cervix:
25	chr17:59628009..59628683-chr6:58777089..58777729,2	MCF-7	breast:
26	chr6:27776232..27779951-chr6:58776955..58780402,3	MCF-7	breast:
27	chr1:110090644..110091238-chr6:58776881..58777871,2	MCF-7	breast:
28	chr6:58772384..58775379-chr6:58777406..58779060,3	K562	blood:
29	chr6:58777671..58778345-chr6:61909292..61909815,4	MCF-7	breast:
30	chr6:31849956..31851616-chr6:58776203..58778751,2	MCF-7	breast:
31	chr6:58777707..58778511-chr6:61909313..61909813,2	MCF-7	breast:
32	chr3:62439844..62440394-chr6:58777335..58777888,2	MCF-7	breast:
33	chr6:58776711..58777237-chr8:105771574..105772190,2	MCF-7	breast:
34	chr6:58776722..58778356-chr8:48323824..48325324,2	MCF-7	breast:
35	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
36	chr21:9826269..9827015-chr6:58776389..58777037,2	MCF-7	breast:
37	chr20:52238301..52240090-chr6:58777406..58779226,2	MCF-7	breast:
38	chr3:90450072..90451589-chr6:58776092..58777719,4	MCF-7	breast:
39	chr13:20943879..20946266-chr6:58777671..58779217,2	MCF-7	breast:
40	chr21:35272607..35275458-chr6:58776178..58778758,2	MCF-7	breast:
41	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
42	chr6:58777390..58779179-chr6:133135024..133136911,2	MCF-7	breast:
43	chr3:63980131..63982580-chr6:58776275..58779243,2	MCF-7	breast:
44	chr3:90451071..90451591-chr6:58777202..58777887,2	MCF-7	breast:
45	chr22:32301912..32302764-chr6:58776740..58777661,2	MCF-7	breast:
46	chr20:36661511..36663112-chr6:58773928..58776889,2	K562	blood:
47	chr18:73688396..73689210-chr6:58777841..58778684,2	MCF-7	breast:
48	chr6:58776657..58777247-chrX:136737324..136737914,2	MCF-7	breast:
49	chr14:98326171..98326823-chr6:58778365..58778943,2	MCF-7	breast:
50	chr6:58775915..58778901-chr8:144691705..144693500,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000141367	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000104524	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000207708	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000026103	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000237080	chromatin interactions
ENSG00000255326	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000160973	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000111321	chromatin interactions
ENSG00000159202	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000226137	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000171858	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000184436	chromatin interactions
ENSG00000207713	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000101407	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000089351	chromatin interactions
ENSG00000126749	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000268858	chromatin interactions
ENSG00000257084	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000140553	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000185158	chromatin interactions
ENSG00000103528	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000248278	chromatin interactions
ENSG00000101413	chromatin interactions
ENSG00000184348	chromatin interactions

Extended variants
information (count: 2000 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2000 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536619756	chr6:58775029-58775030	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs558142417	chr6:58775031-58775032	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs113380148	chr6:58775032-58775033	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs76111939	chr6:58775034-58775035	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs570146881	chr6:58775039-58775040	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs6902762	chr6:58775043-58775044	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs553435026	chr6:58775055-58775056	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs546669458	chr6:58775059-58775060	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs113260866	chr6:58775060-58775061	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs557399492	chr6:58775070-58775071	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs374428629	chr6:58775071-58775072	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs546354060	chr6:58775076-58775077	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs564455090	chr6:58775080-58775081	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs74942959	chr6:58775083-58775084	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs190836144	chr6:58775084-58775085	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs11211719	chr6:58775085-58775086	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs541310647	chr6:58775088-58775089	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs111546137	chr6:58775095-58775096	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs113052707	chr6:58775097-58775098	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs75456522	chr6:58775098-58775099	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs112440970	chr6:58775099-58775100	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs62412781	chr6:58775107-58775108	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs559394856	chr6:58775109-58775110	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs111266149	chr6:58775112-58775113	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs6902944	chr6:58775121-58775122	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs34632346	chr6:58775124-58775125	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs548104122	chr6:58775125-58775126	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs80275999	chr6:58775127-58775128	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs563008785	chr6:58775128-58775129	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs11211721	chr6:58775136-58775137	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs551880198	chr6:58775137-58775138	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs570109248	chr6:58775138-58775139	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs6932072	chr6:58775144-58775145	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs538012648	chr6:58775149-58775150	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs75615646	chr6:58775150-58775151	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs113212764	chr6:58775151-58775152	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs557916644	chr6:58775152-58775153	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs6915033	chr6:58775153-58775154	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375975203	chr6:58775154-58775155	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs575940823	chr6:58775158-58775159	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs183338539	chr6:58775160-58775161	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs375740778	chr6:58775161-58775162	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs188418321	chr6:58775163-58775164	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs539939026	chr6:58775167-58775168	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs558325803	chr6:58775168-58775169	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs573152507	chr6:58775177-58775178	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs193020172	chr6:58775180-58775181	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs74883760	chr6:58775185-58775186	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs574657115	chr6:58775187-58775188	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs141929371	chr6:58775188-58775189	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	5 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:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58775200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:58773400-58775200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:58773400-58775200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
4	chr6:58773400-58775400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
5	chr6:58773400-58775400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
6	chr6:58773400-58775600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
7	chr6:58773400-58775600	ZNF genes & repeats	Liver	Liver
8	chr6:58773400-58775800	ZNF genes & repeats	HMEC	breast
9	chr6:58773400-58776000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:58773400-58776000	ZNF genes & repeats	NH-A	brain
11	chr6:58773400-58776200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:58773400-58776200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:58773400-58776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:58773400-58776400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
15	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
16	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
17	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
18	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
19	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
20	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
23	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
25	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
26	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
27	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
28	chr6:58773600-58775200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:58773600-58775200	ZNF genes & repeats	HepG2	liver
30	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells from cord blood	blood
31	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:58773600-58779200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
33	chr6:58773600-58779400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
34	chr6:58773600-58779400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr6:58773600-58779400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr6:58773600-58779400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr6:58773600-58779400	ZNF genes & repeats	Primary B cells from cord blood	blood
38	chr6:58773600-58779400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
39	chr6:58773600-58779400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:58773600-58779400	ZNF genes & repeats	Fetal Intestine Large	intestine
41	chr6:58774000-58775200	ZNF genes & repeats	Psoas Muscle	Psoas
42	chr6:58774800-58775800	Weak transcription	HSMMtube	muscle
43	chr6:58774800-58776400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:58774800-58776400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:58774800-58776400	Weak transcription	Brain Germinal Matrix	brain
46	chr6:58774800-58776600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:58774800-58776600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr6:58774800-58776600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:58774800-58776600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr6:58774800-58776600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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