Variant report

Variant	esv1004827
Chromosome Location	chr17:18227768-18233875
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:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18158849..18161472-chr17:18226331..18228845,2	MCF-7	breast:
2	chr17:18233805..18235571-chr17:18249290..18250884,2	K562	blood:
3	chr17:18230057..18232102-chr17:18240887..18242532,2	K562	blood:
4	chr17:18042115..18044970-chr17:18226720..18228381,2	MCF-7	breast:
5	chr17:18223830..18226136-chr17:18229956..18231632,3	MCF-7	breast:
6	chr17:18228483..18234046-chr17:18234126..18237765,7	K562	blood:
7	chr17:18229026..18230559-chr17:18233647..18235294,2	MCF-7	breast:
8	chr17:18217609..18225680-chr17:18226125..18232187,14	K562	blood:
9	chr17:18229628..18231978-chr17:18243132..18244767,2	MCF-7	breast:
10	chr17:18229026..18230559-chr17:18233647..18235294,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMCR8-1	chr17:18228890-18231369	NONHSAT146178
2	lnc-SMCR8-1	chr17:18227536-18229211	ENSG00000267350.2

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SMCR8	hsa-miR-19b-3p	chr17:18231326-18231332
2	SMCR8	hsa-miR-130b-3p	chr17:18231312-18231334
3	SMCR8	hsa-miR-19b-3p	chr17:18231312-18231333
4	SMCR8	hsa-miR-130b-3p	chr17:18231327-18231333

Variant related genes	Relation type
ENSG00000177731	chromatin interactions
ENSG00000176994	chromatin interactions
ENSG00000176974	chromatin interactions
ENSG00000177302	chromatin interactions
ENSG00000091536	chromatin interactions

Extended variants
information (count: 218 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:218 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531225261	chr17:18227785-18227786	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs538749401	chr17:18227792-18227793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs547832873	chr17:18227799-18227800	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs188582444	chr17:18227800-18227801	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs563761680	chr17:18227802-18227803	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs558339267	chr17:18227809-18227810	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs374187171	chr17:18227818-18227819	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs34761022	chr17:18227839-18227840	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs368164919	chr17:18227855-18227856	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs534425467	chr17:18227872-18227873	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs181378372	chr17:18227884-18227885	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs574294653	chr17:18227892-18227893	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs184428832	chr17:18227976-18227977	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs556529441	chr17:18227984-18227985	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs576411117	chr17:18227995-18227996	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs545095408	chr17:18228030-18228031	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs34140807	chr17:18228034-18228035	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs114718667	chr17:18228121-18228122	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs567821812	chr17:18228132-18228133	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs371956630	chr17:18228163-18228164	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs527467967	chr17:18228186-18228187	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs540856505	chr17:18228203-18228204	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs560998544	chr17:18228217-18228218	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs139810193	chr17:18228263-18228264	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs530019279	chr17:18228313-18228314	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs533680094	chr17:18228321-18228322	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs375020980	chr17:18228322-18228323	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs554067255	chr17:18228343-18228344	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs571052664	chr17:18228356-18228357	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs74979460	chr17:18228398-18228399	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs189354035	chr17:18228417-18228418	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs149666800	chr17:18228576-18228577	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs4925172	chr17:18228605-18228606	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs534397999	chr17:18228630-18228631	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs144472422	chr17:18228653-18228654	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs180907178	chr17:18228838-18228839	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs148434050	chr17:18228906-18228907	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs576477986	chr17:18228962-18228963	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs115080682	chr17:18228969-18228970	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs142910274	chr17:18228998-18228999	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs4925173	chr17:18229057-18229058	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555694549	chr17:18229074-18229075	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs187008379	chr17:18229100-18229101	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs572563952	chr17:18229111-18229112	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs189384537	chr17:18229112-18229113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs572230364	chr17:18229131-18229132	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs540835615	chr17:18229149-18229150	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs567346062	chr17:18229201-18229202	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs561147865	chr17:18229248-18229249	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs111817220	chr17:18229282-18229283	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Sezary syndrome	18413736	CNVD
Medulloblastoma	16783165	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18219400-18266000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr17:18220200-18228000	Weak transcription	Fetal Kidney	kidney
3	chr17:18220400-18228000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr17:18222400-18266200	Weak transcription	Small Intestine	intestine
5	chr17:18222600-18240800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr17:18222600-18243200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr17:18222800-18236800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr17:18223000-18228200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr17:18223400-18228400	Strong transcription	Primary B cells from cord blood	blood
10	chr17:18223400-18235400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr17:18223600-18240800	Strong transcription	Fetal Muscle Leg	muscle
12	chr17:18223600-18265400	Strong transcription	Fetal Stomach	stomach
13	chr17:18223800-18229200	Strong transcription	NHEK	skin
14	chr17:18223800-18236800	Strong transcription	Primary T cells from cord blood	blood
15	chr17:18223800-18236800	Strong transcription	Lung	lung
16	chr17:18223800-18240800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr17:18223800-18253600	Strong transcription	Thymus	Thymus
18	chr17:18224000-18231000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
19	chr17:18224000-18236600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr17:18224000-18236600	Strong transcription	Fetal Intestine Large	intestine
21	chr17:18224000-18236800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr17:18224000-18240800	Strong transcription	Dnd41	blood
23	chr17:18224200-18228000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr17:18224200-18228200	Strong transcription	Fetal Intestine Small	intestine
25	chr17:18224200-18229400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr17:18224200-18230200	Strong transcription	Brain Anterior Caudate	brain
27	chr17:18224200-18234600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr17:18224200-18235600	Strong transcription	Esophagus	oesophagus
29	chr17:18224200-18236200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr17:18224200-18236400	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr17:18224200-18236600	Strong transcription	Rectal Smooth Muscle	rectum
32	chr17:18224200-18236600	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr17:18224200-18240800	Strong transcription	Fetal Muscle Trunk	muscle
34	chr17:18224200-18253000	Weak transcription	Fetal Heart	heart
35	chr17:18224400-18227800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr17:18224400-18249400	Weak transcription	K562	blood
37	chr17:18224600-18228000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr17:18224600-18236400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr17:18224800-18228400	Strong transcription	Primary B cells from peripheral blood	blood
40	chr17:18224800-18229000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr17:18224800-18229600	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr17:18224800-18236600	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr17:18224800-18236800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr17:18224800-18240600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr17:18224800-18240800	Strong transcription	Fetal Brain Female	brain
46	chr17:18224800-18241000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr17:18224800-18241000	Strong transcription	Adipose Nuclei	Adipose
48	chr17:18225000-18228800	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr17:18225000-18233000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr17:18225200-18228400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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