Variant report

Variant	nsv482159
Chromosome Location	chr11:65122282-65125082
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:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65045328..65049022-chr11:65119140..65122878,4	MCF-7	breast:
2	chr11:65121664..65123613-chr11:65147869..65150112,2	MCF-7	breast:
3	chr11:65110991..65113816-chr11:65120865..65125095,4	MCF-7	breast:
4	chr11:65122004..65123879-chr11:65220475..65223059,2	K562	blood:
5	chr11:65099718..65102956-chr11:65121267..65125924,4	MCF-7	breast:
6	chr11:65123915..65126225-chr16:67902561..67904082,2	K562	blood:
7	chr1:202776745..202779308-chr11:65120833..65122777,2	MCF-7	breast:
8	chr11:65099781..65103974-chr11:65120675..65126515,7	MCF-7	breast:
9	chr11:65088058..65090877-chr11:65123140..65125273,2	K562	blood:
10	chr11:65120584..65123151-chr11:65148447..65152021,3	K562	blood:
11	chr11:65119888..65122132-chr11:65123050..65125503,3	K562	blood:
12	chr11:65123191..65124692-chr11:65148640..65151111,2	K562	blood:
13	chr11:65122241..65124654-chr11:65375609..65378209,2	MCF-7	breast:
14	chr11:65123264..65125729-chr11:65322609..65324877,2	K562	blood:
15	chr11:64971476..64974012-chr11:65120745..65123474,2	K562	blood:
16	chr11:65082018..65083571-chr11:65121331..65123313,2	MCF-7	breast:
17	chr11:65122594..65124302-chr11:65342369..65344295,2	MCF-7	breast:
18	chr11:65105171..65109589-chr11:65119360..65123181,4	K562	blood:
19	chr11:65122242..65122800-chr12:72057275..72057819,2	Hela-S3	cervix:
20	chr11:65101225..65104158-chr11:65123210..65125603,2	K562	blood:
21	chr11:65084600..65086404-chr11:65120200..65124254,3	MCF-7	breast:
22	chr11:65106450..65111070-chr11:65119360..65123401,6	K562	blood:
23	chr11:65116402..65157784-chr11:65261420..65278410,154	K562	blood:
24	chr11:65122441..65125170-chr11:69458785..69461711,2	MCF-7	breast:
25	chr11:65122121..65122705-chr3:138327239..138327942,2	Hela-S3	cervix:
26	chr11:65122123..65123729-chr11:65123796..65125400,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000173442	chromatin interactions
ENSG00000102898	chromatin interactions
ENSG00000117139	chromatin interactions
ENSG00000173727	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000133884	chromatin interactions
ENSG00000149798	chromatin interactions
ENSG00000173825	chromatin interactions
ENSG00000162241	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000173327	chromatin interactions
ENSG00000014216	chromatin interactions
ENSG00000133858	chromatin interactions
ENSG00000158234	chromatin interactions

Extended variants
information (count: 127 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:127 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542628407	chr11:65122305-65122306	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs562903987	chr11:65122307-65122308	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs576565748	chr11:65122476-65122477	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs545515483	chr11:65122487-65122488	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs565406164	chr11:65122499-65122500	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs527466789	chr11:65122510-65122511	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs369749574	chr11:65122519-65122520	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs560994853	chr11:65122540-65122541	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs530002995	chr11:65122652-65122653	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs1018853	chr11:65122682-65122683	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs77130160	chr11:65122694-65122695	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs538297846	chr11:65122709-65122710	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs34591501	chr11:65122812-65122813	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs558770226	chr11:65122918-65122919	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs376715313	chr11:65122927-65122928	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs551835752	chr11:65122961-65122962	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs565473759	chr11:65122974-65122975	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs183187850	chr11:65122983-65122984	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs533211281	chr11:65123070-65123071	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs187118421	chr11:65123151-65123152	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs575636518	chr11:65123180-65123181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs536962368	chr11:65123186-65123187	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs192976354	chr11:65123198-65123199	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs200612846	chr11:65123239-65123240	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs612392	chr11:65123246-65123247	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs199643454	chr11:65123270-65123271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs113056483	chr11:65123271-65123272	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs572592205	chr11:65123337-65123338	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs375954513	chr11:65123339-65123340	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs201019323	chr11:65123385-65123386	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs370523148	chr11:65123388-65123389	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs145214049	chr11:65123393-65123394	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs137952995	chr11:65123441-65123442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs142471374	chr11:65123463-65123464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs540819419	chr11:65123474-65123475	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs144643341	chr11:65123488-65123489	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs138275061	chr11:65123491-65123492	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs149604674	chr11:65123502-65123503	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs554447515	chr11:65123512-65123513	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs371000220	chr11:65123517-65123518	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs375688014	chr11:65123551-65123552	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs373026238	chr11:65123576-65123577	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs202146837	chr11:65123590-65123591	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs529884642	chr11:65123601-65123602	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs372376380	chr11:65123631-65123632	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs375406361	chr11:65123640-65123641	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs367746409	chr11:65123664-65123665	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs144413848	chr11:65123667-65123668	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs543701258	chr11:65123668-65123669	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs372749167	chr11:65123700-65123701	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65121000-65123400	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr11:65121200-65122600	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr11:65121200-65122600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:65121200-65123000	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr11:65121400-65122600	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr11:65121400-65123000	Active TSS	Brain Angular Gyrus	brain
7	chr11:65121400-65123200	Active TSS	H9 Cell Line	embryonic stem cell
8	chr11:65121400-65123400	Active TSS	Fetal Brain Female	brain
9	chr11:65121400-65123600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr11:65121600-65122400	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr11:65121600-65122600	Active TSS	H1 Cell Line	embryonic stem cell
12	chr11:65121600-65122600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:65121600-65122600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:65121600-65122600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:65121600-65122600	Active TSS	Brain Germinal Matrix	brain
16	chr11:65121600-65122600	Active TSS	Ovary	ovary
17	chr11:65121600-65122600	Active TSS	Right Ventricle	heart
18	chr11:65121600-65123000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr11:65121600-65123000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:65121600-65123000	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr11:65121600-65123000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:65121600-65123000	Active TSS	Colon Smooth Muscle	Colon
23	chr11:65121600-65123000	Active TSS	Fetal Brain Male	brain
24	chr11:65121600-65123000	Active TSS	Right Atrium	heart
25	chr11:65121600-65123200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr11:65121600-65123200	Active TSS	HSMM	muscle
27	chr11:65121600-65123400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:65121600-65123600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:65121800-65122400	Active TSS	Fetal Muscle Leg	muscle
30	chr11:65121800-65122400	Active TSS	Fetal Stomach	stomach
31	chr11:65121800-65122400	Active TSS	Placenta Amnion	Placenta Amnion
32	chr11:65121800-65122400	Active TSS	Osteobl	bone
33	chr11:65121800-65122600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:65121800-65122600	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr11:65121800-65122600	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr11:65121800-65122600	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:65121800-65122600	Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr11:65121800-65122600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:65121800-65122600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:65121800-65122600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:65121800-65122600	Active TSS	Brain Substantia Nigra	brain
42	chr11:65121800-65122600	Active TSS	Esophagus	oesophagus
43	chr11:65121800-65122600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr11:65121800-65122600	Active TSS	Gastric	stomach
45	chr11:65121800-65122600	Active TSS	Lung	lung
46	chr11:65121800-65122600	Active TSS	Pancreas	Pancrea
47	chr11:65121800-65122600	Active TSS	Rectal Smooth Muscle	rectum
48	chr11:65121800-65122600	Active TSS	Thymus	Thymus
49	chr11:65121800-65122600	Active TSS	K562	blood
50	chr11:65121800-65122600	Active TSS	NHLF	lung

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