Tag | Content |
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EnhancerAtlas ID | HS038-19051 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr6:116550000-116551160 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7.21 | RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 7.24 | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.93 | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7 | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.55 | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 6.82 |
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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 |
GH06I116228 | chr6 | 116550108 | 116551187 |
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Enhancer Sequence | TTTTAATGTT GATATTCCCT AACATTCTGT ATTTGGCTCT CCTTTCTTCT CCTGTTGTCC 60 TTCAGCTCTC TACCACTGGG AAGCTTTTAA CTATCATCTA TATACTGATG GTTGACATTT 120 CCTTGTCTCT GGGCTTCACA TTTCTCTGAC CTTCAGAAGC CCATTTCTAT CTGTCTTCTA 180 AAATCTTCAC ATCCCACAGC CCCAGGGTGG CAGGAAAGTT GATGTGCTTG CAACAGCTCA 240 TTAAATCCCC ATCCCATTTT AGCATGCCCC TCTTCCCATA TTCCATAATT ACATTTTAGT 300 TACTTTTCCA AGCACAGACT TTAACCAAGC TAGTAAGCAA AAACCACAAT TACTTTTGCA 360 CTAACCTAAA AAATCAGTCA TCCTCATTTC TTCCCTCCCT TTTAAGTTGT CCTTCTGTTT 420 TCTCAGGTTT GTCCTCACTA CATTCCCACC ACTGCCCGCA TCATCCCTTG TGTGAAATGG 480 CACAATATTT AAGTCATTGC TCCAAATGGT TAAAGTAAAG TTAATGCAAC TGAGCTGGCT 540 GGGATGGAAG GCACAGCGAG CCAATCACGA AACACAGCAT GGCCTTAGCG AGTCGCACAG 600 GTTTGACGTC AGCGGTTGTC ATGGTAACAG GGGCAAAGAT GCTGATGCCA GTGTCAGTCA 660 GGACTGAGCT CCTCCCTCCA GTCTGATTCC TGCCAGTGCT TAAGGATGTA TGGAGGGGAG 720 AAGCGTCTTC CAAGCAAAAT CTTCATCCTC TGTTCTCTAT CACGTGCAGT GCGTCACCAG 780 ATCCTCGCCA GTGCTGAGGG TGGGGATACG GGGGAATCTC TGACTTGCAA GATTAAATTA 840 TCATTGGAGA GGGAACGTGT CAGCCTTGTT CACCGCAGTG TCGCCAATGC TGCTAGCTCA 900 GTTCCTGCCC CTGCCCACCA TTGGGAGAAT CATGAGCCAA CTCTCTCTGT CTCTCCTCTC 960 TCTCTCTCTG TCTCGTCCCT TGGCCTTAGC TGTCACCAAT ACACTGACTC TGACTCCCAA 1020 ATCTTTCCCT GAGACCTGTT TTCCTGAGTC TCATACGCAG TTCCTCCTCC ACACTAGGCA 1080 GCTCCACTCA GTGTTCTGAT ATCAAGCTTG AGATTCTCCT TCCGCCTAGA AACCAAAAAC 1140 AACCAAACAT GCCGGTCACC 1160
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