| Tag | Content |
|---|
EnhancerAtlas ID | HS108-19140 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr19:2728430-2729820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr19:2728968-2728978 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr19:2728968-2728978 | GTCACGTGAC | - | 6.02 | | MITF | MA0620.2 | chr19:2728964-2728982 | GCAGGTCACGTGACATTT | + | 7.36 | | MITF | MA0620.2 | chr19:2728964-2728982 | GCAGGTCACGTGACATTT | - | 7.36 | | USF1 | MA0093.2 | chr19:2728967-2728978 | GGTCACGTGAC | - | 6.14 | | USF2 | MA0526.2 | chr19:2728964-2728980 | GCAGGTCACGTGACAT | + | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 2728560 | 2728610 | | chr19 | 2728937 | 2729131 | | chr19 | 2728999 | 2729146 |
| Enhancer Sequence | TGTTAGTCAG GCTGGTCTCC AACTTGTGGG CTCAAGTAAT CTGCCCGCCT CAGCCTCCCA 60
AAGTGCTGGG ATTATAGGCG TGAGCCCCTG CTCCGGGCCG GAGTTTTGTT TTTTAAACAG 120
GAAGCTGTCT TGTGTTATCC AGGAACAATC TGTCCAAGCT ATTCCCGGTC TCTACCAGCG 180
CATGAAACGG TTGGCAGGTG CCCCCTCTCC TCCCTGTGTC TCTCTCATGA ACAGGTGGTT 240
GACATAGACC ACCATCACCT GTCCTGGGTC TTCTGTGAGT TGGGCTGGGT GTCTCCCCCT 300
GGGCCCTGTG GACATTGGGA CTGAACCGTT CTCAAGGGTG GGGCCGTCCT GGGCACTGCA 360
GGGTGCCGAG CAGCATCCCT GGCCTCCACC CACTCCATGC CAGGAGCTCC CCTAGTCAAG 420
ACAACCACAG ATGTCCCCAG ACATGGCCCG GTGTCCCCTG GGGGCAGAAG ATCCCCGGCT 480
GGGAGTCACA GAGTCAGTAA AAGAGACCCC CAAGGAGGAG GACCCTTGGC TTCTGCAGGT 540
CACGTGACAT TTCTGTGACT CAAAGTTGTG TAGAGATGGA GGCGGCCATG TGCAGCTGGA 600
GCTGGCCTGC TCTGCAGTGT CGTGACGTCG TTTTGAGGCA GGAGTAGTCT GTGGCTGCAG 660
GCAGTGACAA ACCCAGGCTT CCTCAAGCAG TGGCTCCTAG CATTGGGTGA CAGTGTGTCT 720
GTGGGCAGAG CCAGAGGAGA CAGAGTCGCT GGGCTGCCTC ACAGGAGCCT GGTCTAGGCC 780
GGACCCGGCC GCCGTCGGCC AAGGGACCTT GGGAATGAGC CCTGCGCCTC TGGACTCTAT 840
ATCGGATGGG CGAGACGACC ACTCCACGTC TTTACCCCAA CATGGACATG TGCTGGGTTC 900
CTCCTCAAAA GCGGGTAAAG CCCCCAGGCG CGGTGGCTCA CGCCTGTAAT CCCAGCACTG 960
TGGGAGGCTG AGGTGGGTAG ATCACCTGAG CTCAAGAGTT TGAGACCAGC CTGACCAACA 1020
CGGTGAAACC CCGTCTCTAC TAAAAATACA AAATTAGCCG AGCGTGGTGC CGGGCACCTA 1080
TGGTCCCTGC TACTCAGGAG GCCGAGGCAG GAGAATCACT TGAATCCGGG AGCAGAGGTT 1140
GCAGTGAGCC GAGATCATGC CACTGCACTC CAGCCTGGGA GACAGAGCGA AACTCCATCT 1200
CAAAAAAAAA AAAAAAAAAG TGGGCCGGGC ACAGTGGCTC ACACGTGTAA TCCCAGCACT 1260
TTGGGAGGCC GAGGCCAGCG GATCACAAGG TCAGGAGTTC GAGACCAACC TGGCCACCAT 1320
GGTGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCTG GCCGTGGTGG TGCGCGCCTG 1380
TAATCCCAGC 1390
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