| Tag | Content |
|---|
EnhancerAtlas ID | HS056-01506 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr10:982650-984100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr10:983660-983671 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr10:983659-983670 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr10:983660-983670 | TCAAGGTCAT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAACTGTCCG CCCCCCAAAA AACAACAAAA AACCAGATTT ACTATGAGGC AAGAAAGACC 60
CTTAGAAGGT TTTGCTGTGG AGTATCTCCA GCCACAAAAG CCACTCCAAT AGAAACACAA 120
TAAGGAACTG GCCTAGGCAA ATTAGGTGGA AGTATTAAAA TGAAGAATGG TGGTAATACA 180
TTTGAATACT GTGAGTAAAA AAGAACGCAT GAGCTTTTAC AGATACTAAG AAATATACGT 240
GAGTGGGTAA GTAAAAAATA GTAGCATTGA GGAAGGAAAA AAGAAAGCTC TTCTTTACAG 300
TAAAATGCTG ATTAATATAT GAAGAAGAGA TTTTTTTATT TTTATTTTTG GAGACAGGGT 360
CTTGCTCTGT CGCCCAGGCT GGAGTGCAGT GGCGCAATCC CAGCTCACTG CAGTCTCGAC 420
CTCCTGGGCT CTAGTGATCC TCCCGCCTCA GCTTCCCAAG TAGCTAGGAC TACAGGCATG 480
CGCCACCATG CCCAGCTAAT TTTTGCATTT TTTGTAGAGA CGAGGTTTCA TCATGTTGCT 540
CAGGCTGGTC TCGAACTCCT GGGCTGAAGC AATCCGCTTA CTTCGACCTC CCAAAATGCT 600
GGGATTACAG ATGTGAGCCA CCACACCTGG CCAGAATTAT TTTAAAAATC ACTATCTTGT 660
AACCACCAGA ATTCTGGCAG GAATCACAAA TGAATGCTAA AATCATTGGG TGAAACTCTG 720
TTGAGGATAT AGATTATGTA CACCACCTCA AAGCTTATTA ATTGCTTGTT GCTTATTAAT 780
TTCAAAGGGA AAGGAGTATT TTTACAGTGA ACAAATATGT TAGACCCCAT CTGAATCAAG 840
TAATCAATGT TAGCATCACT AATAATGGCG GCCTGACCCC CCCTCCCCCA CACCACTATG 900
TGTCTGCCTC AGTTATATGG TATTCCGGCT AAAATTCACA AACTTATCAC GAGGAACAAT 960
CAGACAAACT CGAAGGACAT TCTGCAAATG ACCCATAATC TTTAAAAATG TCAAGGTCAT 1020
AAAAGACAAT GAACACTTCA GGAAGTTTTC CAAATTATAG GAGACTAAGG AGAGAAGTCA 1080
AGCATGACAT GGGCAAACCT AGATTAGCTC CGAGGTCAGA GGAAACATTC GCTGTGATTA 1140
ACATTACTGG ATTTTATTTT ATTTTATTTA TTTTTATTTA TTTATTTATT TTGAGACGGA 1200
GTCTTGCTCT GTCTCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TACAACCTCC 1260
ACCTCCCGGG TTCAAGCGAT TCTCGTGCCT CAGCCTCCTG AGTAGCTGGG ACTACAGGCA 1320
CGCACCACCA CACCTGGCTA ACTTTTTGTA TTTTTAGTAG ACAGGGTTTC TTCATGTTGT 1380
CCAGGCTGGT CTCGAACTCC TGGACTCAAG TGATCTGCCT GCCTCAGCCT CCCAAAGTGC 1440
TGGGATTACA 1450
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