Tag | Content |
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EnhancerAtlas ID | HS176-12030 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:110667060-110668240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr13:110667914-110667925 | TTTTATTGCTT | - | 6.32 | CUX1 | MA0754.1 | chr13:110668222-110668232 | TTATCGATTA | - | 6.02 | CUX2 | MA0755.1 | chr13:110668222-110668232 | TTATCGATTA | - | 6.02 | MEF2A | MA0052.3 | chr13:110667925-110667937 | TTTATTTTTAGA | - | 6.07 | MEF2C | MA0497.1 | chr13:110667924-110667939 | TTTTATTTTTAGATT | - | 6.49 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_36176 | chr13:110662641-110671312 | HMEC | SE_52128 | chr13:110666482-110667281 | Skeletal_Muscle_Myoblast | SE_52128 | chr13:110667367-110668389 | Skeletal_Muscle_Myoblast | SE_63892 | chr13:110666468-110671520 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I110010 | chr13 | 110662562 | 110671114 |
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Enhancer Sequence | CCCTTAGCAT AAGTTTTCAA CCTATGTGTA ATTTATTGGG GTGTGTTGCT CCCAGGCACT 60 CAGGACAGAC AGCGAGGACC TCGGGTTTTG GTTGTGGGTG CTATTGCATG CTGTGGAGAG 120 CTGTGTGTAA CCATGAGTAA ATGCAGACTT AGCAACACCT GTTAGAACCT GGGTGCAGTG 180 GTATCTTTCA ACTTGACGTC AGTGGCACTT TAAATGATTT CAAACAGAAG GGCTCCAGCT 240 GGTCCCAGAG CTGCAGGGTG CCCTTATTAG GATGTGCATC ATATAAATAT AGATGTGTAC 300 ATAACACAAA TATAGATCCC CCTTACAGTA CACTCTGTGC TTGTATTGTT TGCACAGTCA 360 TAAAGAGCCT GCTCATTTTC GGAAGACTGT TTTCCCCCAG GAAATGCAAC ATTTTTTTTT 420 TTTGTTTTTT GCTGTTTCAA TTACAGTTGC AAAGGAAAAC ATTTGAAATG AAAAGTTAAA 480 AATAAAACCA TCATTTCAAG GGAACAATGA AATGTAAGCT CAATGCACAG TAGCATTCTG 540 GTTTTTTTTA ATCTTCAACA AGTGGTTTAA AAAATTAATA ATGTTAAACA TTCGATGAAA 600 TAGGAAATTA AAATGACGTG AGAAACAAAC CCGAGTACAT TAACTATCAT CTGTTTACCT 660 GTCCTAGAGC TAACATGTAA GGCCGAGAAC GTCTGGCAGG AGGCCATGCG ATTGCTTACC 720 ACAAATAAAC CCTGAACTTC TTGAATATCA ACCACCCAAA TCCAGAACCA ACTTACTGTT 780 GCTTTGGCCC AATTCCATGA AACAACTCAT TTCCTTGGGA CTCCATTAGG AAAAATTAAA 840 CTTGCCCCTT TATTTTTTAT TGCTTTTTAT TTTTAGATTA CAAAAGCAGT ATCTGTTCAA 900 TGCAGAAACC TTGGAAAACT AATAAAAACA CAAAGATATT TTTAAAATCA TCTGATACTC 960 ATAATTCCAC TCCCCACTGT TATAATCACC ATTAACATTT TGGTATGTTT CTTTCTGGCT 1020 ACTTTTCTGT GGTCCTTTAC ATATGTCAAT TTTTCCTCCC TGACTGGTGT TTTGCCATGC 1080 ATGCCGTATG GCGCCTACTT CTCACTTAGC AATACATTAT AATCTTTTGC CAAGTTTGAA 1140 ATAACCTTCT CTGGCCTGAT GTTTATCGAT TACATAGTAT 1180
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