| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04274 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr11:94371160-94372960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr11:94371217-94371234 | TGAATTCTTCAAAAGCA | - | 6.35 |
| | | 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 |
| GH11I094637 | chr11 | 94370871 | 94373747 |
| Enhancer Sequence | TAACACTGTG ATGTATTTTA ACCATCAGTT TACACATACT TCTCTCCTGT GAGACTGTGA 60
ATTCTTCAAA AGCAGGTACT GTGTTTAATG AAGTGTGCCC AGGACTTTGC TCAGTGACTG 120
GATGACACAG TAGGAGTAAC AAGAAAGTTC ACATGGGTGA ACCGTGGTAG GTGGACATCG 180
TCTCTCTCAC CTCTTCCCAA ATCAAGGATG AAGTACATCT TCATAAATCC TCATGTGAAT 240
TATTTTGCTA CCTCTAGAAG CATTTTCTAA AACAAGGTGC AGCAATCAGT TGAGTGAATT 300
TGTCACCAGA GCTTATGTTT TCTGAAAGAA CCCTATCCTC AGGCAGTTGT TCCTAAGAGG 360
TGAGTTGTGG ATTTAGTTCA CATACCTTCC TTCGTGGCTT AAAATGCTCC ACATGCCTGT 420
CTCCCCAACA GCATCAGATC ACCATGCAGT AAAATACCAA GTCAGAACAG CCAATGCTGA 480
AAAGAGTGAC AGTTTCCTTT CATGATGCAA TGCACTTGGA GCCAGGGGAC AGGGAGACAA 540
TAACTGCAAG GAGAAGTGAT GACAACCCTA CTTTAATATA GTAGTTCCTT TTGAATTTTA 600
TAGACTTACC CGTTAATCTC TAGAATTTTG AAAAAATTCC TTAAGTGATG TGAGCAAATA 660
ACACTTTGCC TTGGGTTAGC CTTTTCCTTT CCCTTGAAGA TTCCACAAAT ATGTCAGCGC 720
TGGAAATGAT CCTTTGGCTT TGAACTATGT GAAGACTGCA GAAGGACTGG TTGGTAAGCA 780
CCCACATCCT GGGGTGAGAA TCACATCCAG TTTATACCTC CCTGTGCACA CTTGTATAAA 840
ACAACTATAA GACACACGAG AGATCTGGAA GCCAGTTCCT CATAAGTAAG AATTGGTAAG 900
AGCTCTTAAG CAGCATGTCT GAGGTTTAAT AACTCGCCCT GTCTGGAGCC TTTTGTGTGT 960
CTCACTTTCT TCTTAGCAAA ACATGAGCAT TACACTCTGT GCTGGAAGAT TCCCTTCCTT 1020
CTTCCGGGCT TTTGATTACC CAATCCTTCT TTACTTTCAC TTCTTGCTCA AAGCAGCTCT 1080
TTCTCAGCCA TTTCTAAAAA AGGTTTATGA GATGCTGCAG GGCTGTGTCT CTAAATTGGG 1140
CCCTGTGTGC CTATATCCTC ATTCTCTGCA GCTGCTGAAT TCTTTCTGTG GGATCAGCCT 1200
TCTTCTAAGT GCTGGGGTGA TGGGAACATA GCTGTAAACT GATTTTGACA GGAAGCATCA 1260
CTTCCGGCTG GAAACAAGTC CCTGGTTTAT GCAGCACATA GTACTAACTG TGGAACACTG 1320
TTAAACATGT CTCATTCCGC CCCCTCCACC AGCAAAAGGC CTTGCTGCTC AGTTGTGCAC 1380
CAGATGATGT GGCATATGCA CATACTGGCC ACTAATGACA AAGCCTGACA CCATGCAGTG 1440
GACATCTCTT GGGACCTCAG CCTCTTTCTC CTGGAACTGA CCCCATCCTC CCTTCGCTAC 1500
ATGATCACCA TGGGTGGATT CCCAGCAGCC ATGCTTGTAA CATGCATCCT GTCCTCTCTG 1560
GCCACAGACA ACTACAATAC AGATGAGCAG CCCACCCAAG ATTCCTTCTC TAAGAATTTA 1620
GAACTGGGAA TGGAGGAGAG AAAGAGAGAG ATACTGATTC TACCAGAGAC AATGGGATGA 1680
GATAGCATGG TTGTTGGAAC CATGGCTGGA ACTGTAAAGC ACAAATTGGA CAGCAGATAA 1740
AGTTGGTTCA CAGAGAGAGA GAGAATGATG AAGCCATAGG GATCCAAGTT TCCCTATGGC 1800
|
| |
|
|
|
