Tag | Content |
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EnhancerAtlas ID | HS092-14656 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:49469950-49471340 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr13:49470671-49470685 | TACTTCCTGTTTTT | - | 6.74 | SPIC | MA0687.1 | chr13:49470671-49470685 | TACTTCCTGTTTTT | - | 7.47 |
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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 |
GH13I048895 | chr13 | 49470129 | 49471142 |
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Enhancer Sequence | CAAAGTAAAA TCAAATCTGG AAGGCTGAGG CGGGCAGATT GCTTGAGCCC AAGAGTTAGA 60 AACAAGCTTG GGCAACATAG GGAAAGCCCA TCTGTACAAA AAGTACAAAA AATTAGCCAG 120 GTATGGTAGC ATGCATCTGG AGACACAGCT ATTGGGGAGG CTGAGGTGGG AGGACCCCTT 180 GAGCCTGGGA AGTAGATGTT GTAGTGAGCT GTGATGGTGC CACTGAACTC CACCTTGGGC 240 AACAGAGTGA GACTCCGTCT CAATTAAAAA AAAAAATCAA ATCACATTAG AGTTGGAAGA 300 GACCTTAGAG ATGGTCCTGT CCGACCCCCT CAGGTTATAC ATGCACAAAC CAAGGCACAA 360 AGAAATTAGG CAACTTCTCA AAGGTACACA GTCAATAGCT AAGTGGCACC CTCACACACC 420 AATGGGAAGA AGAGGTGATA GGGGTGTTCC CTTACTTCCC GTACAGCCTC GGCTTCATAT 480 AAGGTGAACG AGGGCCTCTC CATCCTGAAT TCTGGGAATG CTCCACCCCT ACTTCCCACT 540 CTCAGCAGGT AAAATGCCCT GATCTGTAGA AGAATTGAGT TTGAGTTGCC TGTGAAACAT 600 CTACATAGAG ATTGCCCAGG AAGCTATTGG ACATAAGGGT AAATAACTTA GGAGCAAGAT 660 CTCAGCAAAG ATGTGGATTC ATGAGTCATC AGTGTACAGC TGAAGATAGG TCCAATTACA 720 ATACTTCCTG TTTTTACATT ATGAATCTGA GACCCAGAAA TGTGATGTAA CTTGACTGGG 780 GCCATATTAG TAGGTACAGA GCAGGGATTT AGAACCTAGT CTTCCTGACT CCCATGTCTG 840 TGCCCCTTCC AAGAGGGCTT GCTGATATGA CTATGTGCTC TGATGAGGAG TGGTAGGAAG 900 GTGTTACAGC AGAGCAATGC TCTTTTAATT TCAATTGCAT ATTTCTATTT CTAATATATA 960 GCTAAACATA AATATGTCTA ATGTGGGTGG CTATACACAT TTTGCAGCTT ATGCAGCCAA 1020 CAAATTGCCT ACTGACAGGC AACCAGCCAC TCACCCTTGT CCTTTGGATA TGATTCCAAC 1080 AAGAAACTCT GTAAAGCTGA GAGAAATCTC ATAATGCCTT CCAGATAGTC CCTTCTGGGT 1140 CCTGTAATCT AACCAAAAGA GTGCAAGATG CCTGCCAGGT ACTGTAATTG GGCCTATCTT 1200 TAGCTATCAA CTGATGATTT CTTTTATAGG AACCTGGTGA CTCCTGACTG TGCTACCCAA 1260 GAAGACTGTG TGGAAGGAAG CAGCAGACAT CAGCATGTCC ATTGCACCAA GACTGGAAGC 1320 CCAACCAGTG ATTTCTGTAG CAATTTCTGA AGTTGCTGAG CAAGTGGATT GAGAGCTTTT 1380 AAGATAACTC 1390
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