Tag | Content |
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EnhancerAtlas ID | HS095-08464 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:49876980-49878490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr13:49877791-49877801 | GGTCACGTGC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 49877360 | 49877515 | chr13 | 49877733 | 49878073 | chr13 | 49878101 | 49878267 |
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| Number: 2 | ID | Chromosome | Start | End |
GH13I049302 | chr13 | 49876497 | 49877462 | GH13I049303 | chr13 | 49877761 | 49878303 |
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Enhancer Sequence | TGAACAACTG GGGGAATTTC AGGGGCATCA GCAGAGCTGG GGAAGCCAGG TGCAGGGAGT 60 GACAGGAAGT CACATGCCAT ATTTTGAACT GTACCTTGGA GAGAGGGAGC CTGAGAGGCA 120 TCCAGCCAGC AGGTGAGTGC ATGCATGAGC TTGGAGATTG CCGAAGTCGG CCCGGAGCCA 180 CAGAGGTGGG AGCCACGGTG GGGCACGCAC AGACCACAGA CCTGAAGCCT TGCAGGAAGA 240 CAGGGAGATG GAGAGGAGAT GCGCAGGAGA CTGAGTCCAG GCACAACGGT GCTCAGTGCT 300 CGGCTCTGAG GTGGAGGAGG CTGAGCTGAG AGAGCACAGG AGGGTGAGGT TGCCTGGGCG 360 ACAGGAGAGG AGAGGGCCTG GAGAAGAGGC CACCAGCTCT GTCACCTGCT GCTGAGGGGT 420 CAGATGAGCA CAGGAAATCG CTACTGGATC TGGTGGCTCT GAGGCCCTGG ATAGCCCTGG 480 GAAGAGCATC TTCCAGGGAG GTGGGGAAGC CAGAGATGGG TGGGTTGTGA GGTACATCAC 540 AGGTGAGGAG GTGTAGCCCA TTCGTGGAGA AATTGGAGAA GTTTTGCCCT GAAGGAGGGC 600 AGAGAGACAG AAAAGGGGCT GGAGGGGCAG CTGAGGGATA AATGGTGCTT TTTTGACGGG 660 TGACGCACAT CTTGTGCAGG AACTACCTGA AAACTTGTGA AGACATTAGA AAGAAGAGCC 720 AAGACCCAAG AAGGGAATTG AAGGTGCGAG GGAAACTGTC ATGCCCGCCC TGCCCTGGCC 780 TTCTTATACG GGTGCCTGTT CCCTGGCTGC AGGTCACGTG CCACATCTTG ATTCTGATGG 840 GCATAGCACA TTGACAACTG AACAAAGCCA CCCGGCTTGG AAATGGTCCC TGGTCAAGGT 900 GAAGGACACG CCTGGTGCTG CCAGAGGCCA CCAGGCAGCT GCAGGCACGC CCTCTTCCTT 960 CCTCCCACAC GCTTGGTAGC ACAGAGCCTC ATTCATCCAG GCCAGCAGGT CACAGCCATG 1020 GGAATGTCAT GCTCAGTTCC CAGGGAAAAG GGCAGAGGCT TTTTCCCCTG CAGAAGAACC 1080 AGTCTGCACC TAGGGCCTTG CCCGTTTTCC CCAAGAGTCC TGTGATTATA TAAGCATCAT 1140 CTGTCCCTGA TGCTGGGGTC CTGGTCAAGA CTTCCCCAGG GCGGGGCTGG GGTGACACAG 1200 CTAGGCCCTG GCCTGGAGTT CAACCACCCT TTGTCCTGAT GGCACTTTAT AAAAACACTG 1260 TCAGCCTGGT CTCTGGGATA ACAGGGTTAC AAGCCTCTGG ATGACTAATT GGCCCTCAGA 1320 ACTAACTGGA TCAAATACAA ACTTTGGGAT GATATTGCGT GCCCCCAGGC CAGGTGGAGA 1380 CCTAGACTGA GCATGGACAC TGCCATGGAG AAAGGACATG GGAACCGTGG GGTCCCCCTG 1440 CTGCCCAGCC ACCCCCACAC CTCGGGTTGA GGTGGGATGT AGGTTACAGA TAAGGTTAAA 1500 ATACAAATGG 1510
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