Tag | Content |
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EnhancerAtlas ID | HS098-16138 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:75941660-75942820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr13:75942011-75942021 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr13:75942011-75942021 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr13:75942011-75942021 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41106 | chr13:75941789-75943916 | Left_Ventricle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 75941916 | 75942023 | chr13 | 75942062 | 75942157 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I075363 | chr13 | 75937751 | 75943074 |
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Enhancer Sequence | AAAAAAAAAA AAAGTTGAGG AAAAACATTA GGGAACAAGT AAACTGAAAA ACTGCCTAAT 60 GAGAAAGAAT AGCAATTTAA ACTAGTCTCA CTCAAACAGA GACAGTATGG AAAAGAAATA 120 TATTTGGTTT GGAAGTAATG CGTGGCTTTA GGGGAAGGGT AGATTTCCTT TATAATTAAT 180 TCTGCTTGTT TAAGAAACCA TTAAGATTAG TTTACAGACT ATCCAGGCAA CACGGGGATG 240 ATGTTGAAAG CGTAATGGTA TGAAGTAAAA TGCAGCATTT TGAGAAACGA TTGATTTGGT 300 CATTTAATGT TATAATTTTT AATTGAGCTT TTTAAAACTT CATCTTCATA TAATGGAAAA 360 TGCTGGGAAG ATATATAGAT GCCAAGTATC AGTTCATTTG TATTCAAGGA AACACTAATC 420 ATTCCTAGCC ATTTTTCCAG CTCCAGTAGC CTTAGAAGCA CACCGAGTTC GTGCTATGGT 480 TTTTAGGGTG AAGCTGTTTG ACAATCTCAT TTTAACTTTT ATCCTAAAAT ACTTCAGAGT 540 TTCTTTGTAT TTAGTTAAAA ATCTAAATTA TTCTTTAAAG CAAATTTTCC AAAGTAAAAT 600 AGAAGTCTAA AACTGAGTCT AGATTCAAAA TAGAATAGAG TAATACACTG ATTTGAAAAT 660 GATAGAACTG TAAAACTGTA AAACTAAGGG TCTCCTTAAG GAATCACCGG TCCCCACTGT 720 CTTATTTTAC AGATGTGGCA ATAAACTGTT AACATCAAAA GTCAAACCAC TGAAGAGGAA 780 AAGAACGAGA TTACAAGAGA CTACACTATT GGGGCCAAAG AAAGCAAGAG TATCTCTGTG 840 ACTTAAACCA GAGTCATACA AGTAGCTTTG TTTTTGATCC TCGGGCTATG AGCCAAGACA 900 GTTTCCTCTC AGACCAGGCT TTAGTTCTTA GATATTCTTG GCAACTTTGC TCCAAACCCA 960 TTTATGGTTC AGCTCTTTTC TAACTGCTGC CTTTTTGATG GCCTCTAAGT TAGGCCAAAT 1020 TGTCAGAGAA ACATTTCTTA AACCATTCTA CTAAGTTCTC TCCTCTCATG CTGTCTCACT 1080 GCTTCTCCAG TTGAATTCCT TCTGTAAAAG GTACGACTTG TGCCTTCTTA TCCTATGACT 1140 GTTACAAATG TGTAAAAGTG 1160
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