Tag | Content |
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EnhancerAtlas ID | HS177-21956 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr7:135397150-135398160 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr7:135398023-135398034 | CTCTGTGGTTT | + | 6.14 |
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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 |
GH07I135712 | chr7 | 135396769 | 135400928 |
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Enhancer Sequence | ACTCCACTGT GTGACCCTAG ACAAGGTATT CAGCCTCTCT GGGCTTCATT TTCTCATCTA 60 AAAAAAAAAA AAAAAAAGGA AGGAAGGTTA TGTGAGTCCC TACCTCATAA GGTTATTACA 120 GAGATTAAAT GACACGTGCA AACCAGCTGG CATGGCCTGC CACATTGATG GCCAGGATCC 180 CTGGTGACTC TTCCTGTTGT GAAGTGCTCC ATCTAAAGGC TGAGCTGGTT TGAGGCCATT 240 AGCACACAGA GTGGGCTCAT CCATGCACAG AGCAAAGCCA CAGGGCTGCT TTTTCATTTT 300 TAGAAATTAA AATTCTGTTC AGTGGTGTTG TTTATTAGTT TTCTAGCCCA TTGATTTTTC 360 TTTCACAATA ACACCTGGGT TATTCAGAGC CTCCCAGGGA ACACCAGACT TCCAAGATTC 420 TCGAGGATGA TTGTTATTGT TTTCTAGAGT GTGTTGCAGA TTTCCTGCCT TTATCAACAG 480 AGCCTGTGCA TTCTCCCCGG CTTCTTGTGA GACATGTGCC AACTCTCCCC ATCATAGCCT 540 CTGCCCAGGG AGCCTCTTAT CGCTCTTGCC CTTGGCTAGC TGTCCAGGCT GCTGGTCCTT 600 CTCTGGTCCC TGGGTCTGCA TTTTGCTGGT TTCCCGTCTC ATTCTTAGGC GGCTGCATTT 660 TCCCGATGTG AGGATGCTTG CCATTAGCAT TCCTTTCCCC ATTTTATAAT TTCCCAGACT 720 CACATCCTGT GAGCTGGGAA GCCAGATAAC GAAGATTGTT AGAGTTTTTT GTAAAGAGAA 780 ATTAGATTCT AAATGGCTGT TCCTCCCCAG GAGTAAAGTG CATGGATTTT AGGACATTTG 840 CATGGTGGTT TGATTGCTTT TTCTGCTTTT CTGCTCTGTG GTTTTTCTCA GTATGCCACA 900 TCACTGAACT TGGAGAGCAG AGGTGTTTCT GGACTGTGTT TTAGGAAAGA TGGGCTCAAG 960 GAGGTCCCCT TGACAAGGAA TAGCTATAGC AATCTTGGGC TCTGAAGTTC 1010
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