Tag | Content |
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EnhancerAtlas ID | HS182-10272 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr18:9493810-9495480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr18:9495014-9495029 | AGGTCTTTGTGACCC | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 9494473 | 9495475 | chr18 | 9494685 | 9495048 |
| | Number: 1 | ID | Chromosome | Start | End |
GH18I009493 | chr18 | 9493899 | 9497660 |
| Enhancer Sequence | GCAATAAAGG TGAAAGACAG TCTTTTGTTA TAATGTTGGA GTACTTTAGA TCTCAGAAGT 60 AGGCCTCAGA AGACAGATCT CTCTCTCTCT GGCCTTCTCC TGGTCTTTGT TCACTTGCTC 120 ATTTTTCTCC CCAAGGCAGG CCATAGAAAC TAAAAACATG CTCTAATCTT CCCCCGGCTT 180 TCTGTCCACA AGCTGGCCAT AAAGGAATTC TCTGACTTAC ATTGTCTGAT TTTAGGTCAT 240 AAGACCCCCA TTTCAAAATG GATCTTGTCC CATACCATGG AGGAAGCAAT GCTGCACAGA 300 GAGGCCAAGA AGAATCTGAA CAAAACAGGC CTTACTGGGT TTCCCCACTC AATCTATTAG 360 TATTAGATTA TACCCTTTTT GTTCAGTCGC ATTTCTGCAT GTTTGTCCAT ACTTCAACAT 420 GCCTATCCAA TGAAGTCTCC ATCAAAAATT TAAGAAGATG GGGTTCCGAG AGCTTTTTGA 480 TTGCAGAACA GGTAGAAGTT CCTGGAGGTT AGTGTAGCCA GAGAGGGCAC GGAAGCTCTG 540 CACTCCTTCC TACATGCCTT GCCCTGTGCA TCTCTTCATC TATACCCTTT GTGTATCCTT 600 TATAATAAAC TGAACATAAG TGTAAACCTA AGTGTATTCC TAGGTTCTGT GAGCTGCTCT 660 AGGAAATTAA TCAAACCCAA GGCAGGGGTC ATGGGAACCA TGATTTATAG CTGGTCCCAT 720 CAGAAGTGTT ACTGGAAAGA TGTCCTGATC AGAACCCAGG ATAGGGTTTT TAGACCTCAC 780 CCAAGAAGGA ATTTGAGGAG AGTCCTTAAA GTGAAAGCAT TAGTTTATTA AGAAAGTAAA 840 GAAAGAAATG AATCGCTACT CCATAGGCAG AGCAGCAGCA TGGGCTGCTC GACTGAATAT 900 ACTTATAGTT ATTTCCTGAT TATGTGCTAA AGAACGGTTA GATTATTCAT GAATTTTCCA 960 GAAAAGGAAT GGGTAATTCC TGAAACTGAG GGTTCATCCC CTTTTTCGAC CATATAGGGT 1020 AACTTCCTGA TGTTGCCATG GCATTTGTAA ACTGTCATGA TGCTGGTGGG AGTGTCTTTT 1080 AGCGTGCTAA TGCATTACAG TTAGCCTATA GTGAGCAGTG AGGATGAGCA GAGGTCACTT 1140 TCATAACCAT CTTAGTTTCG GTGGGATCTG GCCGGCTTCT TAACCACATC CTGTTTTATC 1200 AGCAAGGTCT TTGTGACCCA TATCTTGTGT TGACCTCCAA TCTCATCCTG TGATTAAGGA 1260 TGCCTAACCT CCTGAGAATG CAGCCCAGTT AATCTCAGCC TTATTTTACC CAGCCCCTAT 1320 TCAAGATGGA GTTGCTCTGG TTCAAATATC TCTGACGGAA GCACAGGTAA AACAGCCTAG 1380 GGCTTGCAAT TGGCGTCAGA AGTTGGAGGC GGGCAGCCTT GGGGACTGAG CCGTCAACCT 1440 GTGGAATCTG ATGCTACGGA TGGTGTCAGA ATTAAATTGG AGAACACCCA GCTGGTGTCC 1500 ACTGCAAAGT TGATTGCTTG CTTGGTGGAG TAAACCCCTA TATATCATGG TATAAGAGCA 1560 GAGAAAAAAC TGATTTTCTA CATAATCAGA TTGTTTTGTT TGTTTATTTT TCAGGGATAG 1620 TGTGTGCATC CATCAAGGAG CTCTTCTCTT TCTATCTCTT GCTCTCTTTT 1670
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