Tag | Content |
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EnhancerAtlas ID | HS080-00859 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:37699870-37701620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LBX2 | MA0699.1 | chr1:37700628-37700638 | GCTAATTGGC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I037234 | chr1 | 37700490 | 37701297 |
| Enhancer Sequence | ACATTGTATT ATAAGTAATT CTTTATACAT ACACCGCCTC ACCCCTGGGC TAGATTCTTT 60 GAGGGCAAGA ACTGTATCTT ATTTATCTCT GTACCCTCAA TGCCTTGCAC AAAAGAAGTG 120 TTCAGAAGAT ACATGGTGAA TGCATCAATG CAAAAGTACA TGAATATGGA TGGACAGACG 180 AACAGATGGA TGGGCAGTGG GCAATCTTCC TGTCCACTTC AGCCCAGACT TCAACCCAGC 240 TCTTCCCCAA GTATCTCAGG CTGGCACAAA ACCCAGGCAA TCACTCAAGT GAACAGTAAC 300 ATAGCACAGC TCACCTGGAC TGGAAAGAAA CTGTGGACTC AGAAACCTGA GGTGTAGAAT 360 TTTGAGGATC TCTTGGGGCC AGAGAAAACC ACTTAGGAAG AGCCAGGCTC CTCACAAACC 420 TGCCAGGAGC CTCAATGGGA GAAAATGATT TAATTATCGG AGTGTCACCA AACAAATTGT 480 AAGCCTCATT TTGGGGTACT TAATGCTTAT GGTAATTAAC ATTACGAAGA TTTTTCTTTT 540 CTCTTCTGTT TATATTTGGT TTAGCCATTC ACAATACAGC TAAAATTATT TCGACTAATT 600 TTAGGAGCTC TTTCTACATT GCCCCTGTGT TTCTTCCCCA GCACTGCTAC CCAAATGCAA 660 TCTTTAACTT CAGAGACAGC CAAATGCAGG ACAAATTGGA ATCAATGCTG CCTTTGTCTT 720 CGCTAATAAG TGGCTGCCAC GCAGAGGAGT GTGGAACTGC TAATTGGCTG ATCTCAACAG 780 GGAAGAGACA ATGGTCGCGA GAATGCTGGG AGATTAATTA TAGGGCCGCC TTCTGCGAGG 840 CCTGGCTTCC GCTGCTCCTG GCTCGCGATG CAACAAGGGT GGGCCTCTCC ACCCATCTTT 900 AGAAACAGCA GCCTCTCCAG CTGGAATTCT CCTGCACTGG GGATTCAGAC CACACACCCA 960 GCACACACAA AGGTCAAGGA AGAGGAATGT GGGAGTGGAG GGGGGGAGAC TTCAAATTCA 1020 CAAAGGAAAG CACCAGAGTG TGTGTGCTGG AGGGTGGGAA TGAGGGAGCA CTCACTGGGA 1080 TGTGAAGCTC TGTGCACCTG CTCGTGAGGG AGGCACGATC ATCCCCCAAC ACATGACGAA 1140 ACTGAGGCCT CAAACGGTGA GAAAACTAAA GGATCAAGCT TGCTCAAGTT ATATCAGGTT 1200 AGCTCCTAAA AGGAGGCAAC AGTTCCCTCT TAGAAGCAGC CAAGCTACAA GTAAAGACTC 1260 CTCTGAGCCT GGATTTGAAC TCAACTTTGT CTGATTCCAG AGCCCATATT CTTTGCACTC 1320 TCAAAAGCTC TCCTTCACCA TTAGTCTGTG GCCTCTGAAA CCTGATTTCC TTGTCTTTGG 1380 GGTAAAGGGT TACCTCTGAA ATGTCCTCAT TAAAATGCAA ATATATCTGC AGAGTGGAGG 1440 AGCGAAGGCA TCTCTTAGCC CAGATTTGCT GTTTAAATGA AGCACCTGAC ACCAGGGAAA 1500 GCAGATTCTT CAAGGAATGA GTAACATCAG TTTTGATAAG GGGAAGGGGA ACTGCCAAGA 1560 GACAGCAGGG CCACATGGAA CTCAGTGGTT GTCTTGGGAA TGGGATGGGG AAGCCCAAAG 1620 TGGTGGCATT TGGAAGGAAA ACACCAAAGG GATTGCTTCA AAGGCAAACT GGGCTGAGTC 1680 CAATAATCCC AAATCAAATT TGGTGTTCTC TTCTCAAAAG CCACAGTCTC TCCCGGATGC 1740 CACATCTCTG 1750
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