| Tag | Content |
|---|
EnhancerAtlas ID | HS103-04947 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:130272740-130274810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:130274282-130274303 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Myog | MA0500.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.02 | | RORA(var.2) | MA0072.1 | chr11:130274735-130274749 | CTGACCTAGTTTCA | - | 6.1 | | Tcf12 | MA0521.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_08530 | chr11:130270251-130275391 | Brain_Inferior_Temporal_Lobe | | SE_39023 | chr11:130269984-130274795 | IMR90 | | SE_69174 | chr11:130272967-130276303 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I130400 | chr11 | 130270005 | 130274950 |
|
Enhancer Sequence | TCAGAGAACA GATGCGGATC TAGTGAGATG GGTCCTACCA CCCCTGGAAT ATGTTCCTGG 60
GAGAGGGGTG GTCTGCTAGA GTGGACTGGG AATAGTAATA TTGCATACTT TTGTAAATTC 120
ACAAAACCCT CTGATCTGTG ATAGAGGAAT AAAGGGCAGA GGATAAACCC CAGATAAAGA 180
TTCACTTATC TTAAAAATGA AAGGTTGGAA ATTAACTTTA TGCTACTGTA CCACCTTCGA 240
AGTATTTCTG GCAGGTGCCT GGAGGATTCA GATTAATGAC CAAATTACCT GCCAAGTCAG 300
GGCCTCCCAT TAGAAGAGAG TACCAGTTTC CATTAGGAGC ACTAGCTGGA AAACACAATC 360
TTTCAGCAGA GGAAATACAG TCTTCTCTCC TTCTCTGGGT GCACAGAGTG GTCGTGGTTG 420
GCTGGGGCAG ATAATGGTGT GGTCTTCCTC TGCAGATCTG GTTTCTGAGT CCCTGGGCTG 480
CAGCTGTTGA ATTTCCAGAC ACAAACAAGT ATGCGTTCTG AGAGCCTCGC CGAGCCCACA 540
CAACCGGGAG AGCCAAGCTG GATTCCATTC TGCTTTGCAC ATCAGCAGCT CTGCTGCCAG 600
CTGAACTCCA GGGCAAAAGC TGTGCCTGGT AATGATGCAG GCAGCAGGGA TGGCACAGCT 660
GGCCTGGCTT AGGCCGTTAA GGGGGACACG CTTGGCCTTA TTTGGGGGAG AGCGAGAAAT 720
GGAAGGCGAT GAAGAGTTGC GGAAGCATAC ATCAGCCTCC ACAAAACTGG TGCACAGCAG 780
GGAAACAATC TGGTTTTGCT AGTCATCAAC AACATGCCTG TGTGTGTGCC TGTTTATGCT 840
TAGGTAAGCC CAGCCTCCCA CTCGCTGAAA AGAGTAGGCA GACAAGAAGG AGTGACCAAC 900
TCTGAGTCAG CTGTCATCGT GTAGAGAGCA GCTAAGGGGA ACAGTGGGGC TGGAATCTCA 960
TGGCCTTGCC TAGTGCCCCT ACAGCATCCT CTCTGCCCAT GGTGCCAGAT ATCTGAATGG 1020
GAGGACAAAG GGGGCACAGG TGGTGAAAAA AACCAAGATG CACATTTGGG TATTTTCCTT 1080
CTTTTGCTAG AATGTCATTT CTTGATGTCT GTTTCTTGTC ACCCATTTGT GATCAGGGAC 1140
TAAGTAAGTT CCCTCTGCAC CAGACCAGGT GGAAGACTGA GCCAGAGTTC CTCTGAGCCA 1200
CAGGAGAGAT GAGGAGCTAT GGAGCGGAGT AGGGGCTGAG GATCTGGTGC CCCCAGCTAA 1260
ACTAAAAGGA GGCAGGCAGC ATGTAAGAGG ATGATGGGGT AGCTCACAGA GAGGAAGGGG 1320
ATATTCTTTC TCAAGAATGA TGAGCCCAAA GGCATCGCAT AACAATTGTG ATCTCCCAGC 1380
TGGACGTTTC CTGTAGCACA GGTGTTCACA GTGTGGCTCC CAAACCAGCA GCCTCCATGT 1440
CAGTCACTGG GAACTTGTTA GAAATGCAGA TTCTCAGGCC ACCCCAACCA TTAGATCAGA 1500
AACTCTGGGG ATGGGGCCCC ACAATCTGTG TTTTCTTTTC TTTCTTTCTT TCTTTTTTTT 1560
TTTTTTTGAG ACAGGGTCTC ACTGTGTCAT CCAGGCTGGA GTGCAGTGGC ATGAAAATGG 1620
CTCACTGCAG CCTCAACCTC CTGGGCTCAA GTGACCCTCC CACCTCAGCC TCCTGAGTAG 1680
CTGGGACTAC AGGCCTGTAC CACCATGACC GACTGATTTC GTTTTTTAAT TTTTTATAGA 1740
AACAGGGTCT CGCCATATTG TCATGGCTGG TCTTGAACTC CTGGGCTCAG GCAATCCTCC 1800
TGCCTCAGCC TCCCAAAGTG CTGGAATGAC AGGTGTGAGC CACTGTGCCC AGCCTCACAA 1860
TCCATTTTCA CAGCCCTCTA CGTGATCCTA ATGAAACCTT GGGAACCACT GGTCTAGATC 1920
CTGCAAATGA AAGTTGCCCG AATGAGCTGG ATTCTGCAGG CCTGTGAGGA CCCAGAGCAG 1980
GCAGGGATCC AGCTGCTGAC CTAGTTTCAG CCTCCATCCC TGGGTTCTAG GTTGCTGCCC 2040
TTTCCAAAGA AACAATGAAT CAGACCAGAC 2070
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