Tag | Content |
---|
EnhancerAtlas ID | HS182-00910 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:54560490-54561950 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr1:54561469-54561480 | TCCTTATCTGT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 54561536 | 54561938 | chr1 | 54561659 | 54561839 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I054093 | chr1 | 54559506 | 54563052 |
| Enhancer Sequence | TTTTCTACTA GGAGAGACAA ACTTAAAATA TAGATCATTG GCTGGGTGCA GTGGCTCATG 60 CCTGTAATCT CAGCACTTTG GGAGGCCAAG GTGGGAGGAT TGCTTGAGGC CAGGAGTTCA 120 AGACCAGTCT GGGCAACATA GCAAGACCCC ATCTCTAAAT TTTTTTTTAA TTTTAATTAG 180 CGGAGCATGG TGGTGCATGC CTGTAATAAT CCTAGCTCTT GAGAGGCTGA AGCCAGAAGA 240 TCACTTGAGC CCATGAGTTT GAGCCTGCAG TAAGCTTTGA TCACACCACT GCACTCCAGC 300 CCAGGTGACA GAGTGAGACA GTATCTGTAA AATAAAAGTA TATACTTCAT TTATAATATA 360 TGATGATAGT GACTAAGGGA AGCTCAGGGC ATGGTGGCAG CCTGAAGAGC TTTCAGTCCT 420 TTGCACTGGG GTCTTTTTGT TTGGTTGTTT TTGCCTCGGC TTTGACATAC AAAGAGGAGT 480 GTTTTCCGTA GGGAAAGGTG TGCCTTGCTA AGGGAACATG TGCTGGTGCA GAGGCACAGA 540 GGTGTGTGAA AGTGGTCAAG AGTGGAGTGC TCAGGGCCAG GTGTGGTCAG GATTGGGGAG 600 GGGAATAGCT GAAGATGGGC CTGGAAAGGA GGGTAGGGGC TGGGGGGTCT CGGATCAGCA 660 TCCCAACCTA CCCTGGATTC AGACCGTGTA GACAAAGTTC CAGATCTCTC CTGCTTTGAT 720 TAGGTCTGGG ACCTCAAGAT GGCTTGGGCC TGAGCCAGAC CACCCCAGAA TTGCTACAGT 780 TCCCTTCCCT AGACCTGCTC TGCTTAATGG AAACTGTAGG CGTCTCTCCA ATCTCAACCA 840 TTCTCTCGGA ATGTTGAAGG GGCCATTAGT ATGGTGAAAG GGAAGAAACA TGAACTTTGG 900 AGTCGAGGGG TCCAGGTCAC AGTCCCAGCT CTGTCTCTTA GTAATTGTAA GACCTTGAAC 960 CTTTGCCTTT GAACCTATTT CCTTATCTGT AAAATGTGAT AATAGGAGTT ATGAGCATTA 1020 AATGTGAAAA GTGATTTTTG AACTGTTCTG TACACATATT AGGATCTAGA CCCCATGTCT 1080 CTAAAATGCC GTAAGGAGTT AAAAGGCAGT CTAAAAACAA AACAAAAAAA AATATGAACC 1140 GTTATACTGA TTTATTATTC TTGGTCTTCG TTTCCTGGTT GGTAAAGTAC AGGGCCCAGT 1200 ACCCGTTGCT TAGTTCAGGC CAGTTTCCTG TTATATTACC ACCCGGCAGG GGTTGTGAAT 1260 GAGGTCCCTG TCACAAAGCA CATGGCCTTG TTCCTTAATT GCCAGGGTGG AATTAATTTG 1320 CTCTTCCTGT TTCTCTTGTG ACAGGAAGTA GATGTCCTTG AATTTCAGTT GATTAATGGA 1380 GGCCTCTGAG CAGAGTGCTC CAGCCTCTCT TGCTTTTAAT CCTTACGCAA TGTAAGGCTC 1440 TAATTTGATA ATTTTGCTGT 1460
|
| |
|
|
|