| Tag | Content |
|---|
EnhancerAtlas ID | HS056-16135 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chrX:23835050-23836210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF3 | MA0640.1 | chrX:23835558-23835571 | AACCAGGAAGTGA | + | 6 | | ELF5 | MA0136.2 | chrX:23835592-23835603 | TACTTCCTGGT | - | 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 |
| GH0XI023817 | chrX | 23835221 | 23835917 |
|
Enhancer Sequence | CACCGTGCCC GGCCCTGCTC ATTAGTGTAT TGTATGTGTG GGCAGGTAGG GGGAAGATGG 60
GGTAGATAAA AGACTAACAA ATAAAATATA ATAGAGTGAT AGTGCAACAA GGAAAACAAA 120
ACTACCTTCT CCTGGTTGGT CAGGACACAC CCAAACAAAG GTCAATTTAG GTCAGACCTG 180
GATGACAAGG AGCTAGCCTC ACAAAGTTGT GGGGGCAGTC CTGTGCACTG CGAGATGCTC 240
AGCAGCATCT CTGGCCTCTA CCCACAAGAT GCCAGTAGCA TGCCCCTCCT AAGGTGACAC 300
AACCCAAAAT GCCTAGGGGA CATGATGGCC TGACTGAGAA CCACTGGGTT AAGGCAAGGG 360
CATTCCCAGC AGGAGAAACC AGCAAGTGCA AGGAAGGAAG AAGGCCCCAG CCTGCCTGGC 420
CTCACCAGCT CCCGCTGCCC TGCCTGCTAG GTGAATCTGT CAACTGTGGC AAAGTAGCAA 480
CTGATGCTCA GAGTGGAGAG GGGTAATAAA CCAGGAAGTG AGACTGGCCA ACTGGGGGTG 540
AATACTTCCT GGTTCAACAC TTCAGCTGTG GGCTGCTCAT CTTCCCCACT CACAGTCTGA 600
GACTGAGGCC AGACAGTCTC TGAATACATC AGGGCACACA GTCAAGTAGG TACCATGGGT 660
GAGTCTGGGC TATGTATTGC TTCCCTGAAG AGGACTCCTT GCTGCCCAGG GAACTCAGAG 720
AAGGGCCAGG CAGTCACTTT TCTATCATTT GAGACCAGAT TTTTTCTTTT TTTTTGAGAC 780
ACAATCTTGT TCTGTTGCCC AGGCTGCAGT GCAGTGGCAT GATCTCTGCT CACTGCAACC 840
ATCTGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGAACTACA 900
GGCGTGCACC AGCATGCCTG GCTAATCTTT TTATAATTTT AGTAGAGATG GGGCTTCACC 960
ATGTTGGCCA GGCTGGTCTC CAACTCCTGA CCTCAGATGA TCCACCTGCC TTGACCTCCC 1020
AAAGTGCTGG GATTACAGGC GTGAGCCACT GCACCTGGCC GAGACCAGAT TTTTAGTTGC 1080
TTTTAGCAGC TGCCTTAGTT ACTGGAAAAA GTAAATCCAA ACAACTCTAA CTCAAATTTA 1140
TATCCTGTCA ATTCATTATC 1160
|
