Tag | Content |
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EnhancerAtlas ID | HS058-01274 |
Organism | Homo sapiens |
Tissue/cell | GM10847 |
Coordinate | chr11:3832660-3834070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG1 | MA0623.2 | chr11:3833407-3833417 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr11:3833407-3833417 | GACATATGTC | - | 6.02 | STAT3 | MA0144.2 | chr11:3833051-3833062 | TTTCTGGGAAG | + | 6.02 | Stat4 | MA0518.1 | chr11:3833051-3833065 | TTTCTGGGAAGTGG | + | 6.14 | ZNF263 | MA0528.1 | chr11:3833767-3833788 | TGAGGAGCAGAAGGAGGAGGA | + | 7.48 | ZNF263 | MA0528.1 | chr11:3833776-3833797 | GAAGGAGGAGGAGGAAGAGAC | + | 7.76 | ZNF263 | MA0528.1 | chr11:3833770-3833791 | GGAGCAGAAGGAGGAGGAGGA | + | 8.26 |
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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 |
GH11I003812 | chr11 | 3833340 | 3833454 |
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Enhancer Sequence | CATGGGGACA CTGATACCTC ATATTCAGGC CGATCTGGAT CTTCTTTAGA TCTTGAATAT 60 CTTTTAACAA GATTAGCCAG CTCTCCACTG GGGCCCATCA AACATACGGG GCTGCTGGGG 120 GGATGCCTGC AAATTGAAAT CTCAAGGGTT AGTCTCCCTC TGCCTTCTGT GAGGTTCTGG 180 AGGCTGGAGT CACTGAAGTG TAATATAGAG TCAGTAAATG AATTACAAGT ATAACAGAGT 240 TTGACACATG TCCCACCCCA TTTACTTTGA TATCCTAGAG AAAGTGGTCT TACATCTTTC 300 TTCCTGGCCC CGCGCCCCAT ATCCCTGTCC AGAGGGCAGA CCTAGAGCCA AATCCTTACT 360 TCATAGAAGA GCAGATTCTG GAACCCCAGG GTTTCTGGGA AGTGGAGAGA GAACAGGATT 420 GGGCTAGAGG GTATTTTGGG CCTCTTAATG TAGCACTATG GGCTTGTGCC TGTCTCTGTA 480 GGAATGTGAC TCAGTATATG TGTGTGTGAT TGTGAGGGTC ATGACTGTAT ATAATGGGTT 540 TGAGTGGGTC GTGTGTGAGA GAGACTATAT CTGTGCCTGT CTGTATGGAG ATCTGATTAT 600 GTACGTGTGT ATGTGTCCTG GGGTGAGTCC CGTGGCCTCT AAGATTCCAT AGATGTCTGT 660 GTACCCTCTG GACAGGGATA TGGGGTGCGG GGCCAGGAAG AAAGATGTAA GACCACTTTC 720 TCTAGGATAT CAAAGTAAGT GGGGTGGGAC ATATGTCAAA CTCTGTTATA CTTGTAATTC 780 ATTTACTGAC TCTATATTAC CTGAGACAGA GACCCAGCCT CAGTTTCCTC ATGTCTGAAA 840 TAGAATTGAT TAGCTGGGCA TGGGGGTATG CACCTGTAGT CCTAGCTCCT CAGGAGCCTG 900 AGGTGGGAGG ATTGCTTGAG CCTAGAAGTC TGAGGCTGGA GTGAGCTATG GTTTTCTCAC 960 TGTACTTCAG CCTGATGACA TAGTGAGACC CCCATTTCTA AAAAATAAAA TAGGGTTGAT 1020 AATTCCTGTC CTGCTCCTTC CCAGGGCTAG TGTAGAGCTC TAGGTAGAAG AAGGATAGGA 1080 AGGTAGTTTA GGGAGGATGA TGAAATGTGA GGAGCAGAAG GAGGAGGAGG AAGAGACTGT 1140 CAGGTTGGAA GGCAGGGCAG GAAATGAACT TAACCTAGGG GCTTTAGGTG GAGAAGAGGC 1200 AGATTCTGCG CATGGACCAT TGGGGTCCCT CAGAGTTCTG AAGGCCCCAG CCAGCTGGAT 1260 CCCCACTTCA TGTAAAGAGC ATCTGCTTCA GAGAAATGGC TAGGATTAGC AGTGGGGTCT 1320 AGCTGTGAGT ATGGGGTGGA GCCCCACTTC TTTACTTCAT GTGACTGGAG TTTCCTCTCC 1380 TCCTGATTTG TCAGTGGGTA GACATGGGTG 1410
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