Tag | Content |
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EnhancerAtlas ID | HS177-11667 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr2:30733850-30734850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr2:30734734-30734745 | CTAATCCTCTT | - | 6.62 | FOSL1 | MA0477.1 | chr2:30734159-30734170 | CATGAGTCACC | - | 6.62 | HNF4G | MA0484.1 | chr2:30734025-30734040 | TGAACTTTGGGCTTT | - | 6.09 | JUND | MA0491.1 | chr2:30734159-30734170 | CATGAGTCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 30734376 | 30734545 | chr2 | 30734733 | 30734838 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I030511 | chr2 | 30733965 | 30734547 |
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Enhancer Sequence | TTTGAAGTTT TCTTTTCCCC TGAATAGTTT ATTTCCTTCA AGTATACTTT TTTTTCTGTT 60 TAATTTAGTC TCTAATGTCA TGTTAGAGTG TTTGCTCAGA AGTCTCATTA TCTGTTCCTA 120 ATAAAAAATG GGTGATTTAG AAAGCCAGTA GAGGCTTGCA CGTAGGTGAG GCTTGTGAAC 180 TTTGGGCTTT ACTGAGGGGT GATTTATGTG GGCTGTTTAT TAGGGAATCC CTCAATGTTT 240 CTGTATTTTC GAACTCCTGA CCTCAAGTGA TCTGACCGCC TCGGCCTCCC AAAGTGCTAG 300 GATTACAGGC ATGAGTCACC GCGCCTGGCC TGTTTCTGTA TTTTTGTCTT TCCTCATAGC 360 CTGGTCAGAC ATCCCAGAGA GTACACTCCT GTCTTCTGCC TAGGACTGTG CTGTTCAATA 420 CTGTGGCCAC TACCCACATG TAGCTATTTA AATTGAAATA TAATTAAGTT AAAAATTCAT 480 TTCTTCAATG GCACTAGCCA CATTTCAGAT GCTCAATAGC TACATGTAGC TAATGGCTGC 540 AGTTTTGGAC AGCATAACTA GGGAACATTT CCATCATTGC AGAATATTCT ATAGGACAAC 600 TGGCATAGGA CCAAAGATCT TGTTGCCAGC CATCTGAGAG CTCATCCAGG GAAGATGGTC 660 TGAGGTTTTA GCATTCAGGA TTCAGCATGT ATATGGTCAC TTAATCCCAC TGTTCTTAGA 720 GTGGTGACCA TGCCCTAAAC TGTGCATTTC CTAATTGGGA AACTCTGTTT TACCTTCTCT 780 AGAGAATAGA CATGCAAGTT TATGCTGCGG TAGGAGAGGG ACAGTTACCC AGAGGTGCAG 840 AGAGAGAAGG GAATCTAGGA ATCCACCTGC CCCTCACTCA TTACCTAATC CTCTTTATTT 900 TGGCAAACTG CCATTCATCT CCATTTGCAT CCAGCAGTAC CTGATGCTTC CGCCTCCTAG 960 GCCTTAGGAG GATTCTGTGG GTTTGTTTTC AACTTTTTCC 1000
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