| Tag | Content |
|---|
EnhancerAtlas ID | HS023-17412 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr22:43474310-43475900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr22:43475506-43475517 | AGCTGTGATTT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 43474572 | 43474818 | | chr22 | 43475030 | 43475197 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I043078 | chr22 | 43474601 | 43474770 |
| Enhancer Sequence | GGCCAACATG GGGAAACCCC GTCTCTACTA AAAATACAAA AATTAGCTGG GCGTGGTGGC 60
ATGTGCCTGT AATCCCAGCT ACTCAGGAGG CTGAGGCAGG AGAATTGCTT GAACCCGAGA 120
GGCGGAGGTC ACAGTGAGCC AAGATCGCAC CATTGCACTC TAGCCTGGGC GACACAGCAA 180
GACTCTGTCA GAAAAGAAAA GGAAGGAAAA ACAAAAGAGA AGAGAAGAGA AGAAAAGGAA 240
ACAGACTCAA GGGAGTCCGG GTGCCCTGAT TCAAAGCCGG GATGATACTA CTCTAAAGTG 300
CCGCCTCTCT CCACACAGCC CATCACTTCC CTCTGTGAAC CTGGCCTTTG GCAGGATGAT 360
GACAACACCC AGGTCACAGG GTCAATGAGC AATAAACAGA ACCGCTCTCT GCAAGCTACA 420
AGGTGCTGTA TAAAGGACTG CTGTTAGGTG ATCCGATATG GTGCACGTGG AACCTCAGCA 480
GTCACACCAA GATGACAATA AAAGCACAGG AGCCGCACCC CAGAGCGTGA GCCCATCCCA 540
CACCCCTCAC ACCCACAGAC ACGGGGACCA CGGGAGCCGC ACCCCAGAGC GTGAGCCCAT 600
CCCACACCCC TCACACCCAC AGACACGGGG ACCACGGGAG CCGCACCCCA GAGCGTGAGC 660
CCATCCCACA CCCCTCACAC CCACAGACAC GGGGACCACG GGAGCCGCAC CCCAGAGCGT 720
GAGTCCATCC CACACCCCTC ACACCCGCAG ACAAGGGGAC CACGGGAGCC ACACCCCAGA 780
GCGTGAGTCC ATCCCACACC CCTCACACCC GCAGACACGG GGACCATGGG AGCCGCACCC 840
CAGAGCGTGA GCCCATCCTA CACCCCTCAC ACCCACAGAC ACGGGGACCA CGGGAGCCGC 900
ACCCCAGAGC GTGAGCCCAT CCCACACCCC TCACACCCAC AGACATGGGG GCCAAGGGAG 960
CCGCACCCCA GAGCGTGAGC CCATCCCACA CCCCTCACAT CTGCAGACAC GGGGGCCACA 1020
GGAGCCACAC CCCAGGTGTG AGCCCATCCC ACACCCCTCA CACCCGAAGA CATGGGGACC 1080
ACGGGAGCTG CATCCCAGAG CGTGAGCCGA TTCCACACCC CTCACACCCG CAGACACGGG 1140
GCCACGCCAA TGGCTCAGGG AACTTTTCAT TTTCACTATG TGATTTCAGC CTCCACAGCT 1200
GTGATTTCCT GATGAATCCT GCTTGCGGCC TGGGGACCAC CCCCCAACCA CCGCCGTCCA 1260
GGCTGCATGG TTCACATGTT GTACTTAAAG CAAGCATCTT AGTGGGTGAC CTCACACCAG 1320
CCACTGACAT CTACCTGGAG GTGACAGAAG AGTAGTGACT GGAGACCAGG AAGGCTGTGC 1380
GCGATTCTCA CACAGTGCTT CCCCAGGCCT CAACGCTTTC AGGTGTGAGA CCCCAAACCT 1440
ACCGAGGCAG ACGGGCCAAA CATCCTCATC CACATTTCAC TAAGCAACTG GGGCAGGTGC 1500
TTTAGCCAGA CCATCAGGTG TCCCTCCCAG GCCCCGCGCC CTCTCTCCCA CCGTGTGGGC 1560
AAATGGTCCC TAAGGGGCCG TCTCAGGCTG 1590
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