Tag | Content |
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EnhancerAtlas ID | HS018-00446 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:31455230-31456680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:31456173-31456186 | TTCTGGAATTTTC | + | 6.17 |
| | 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 |
GH01I030982 | chr1 | 31455248 | 31456247 |
| Enhancer Sequence | GTATTGGTAT AAAGAAAGGG GATGCCAGTA ACCTAATTTG TGGATCACCT TAATGGGCCT 60 CCTTCCAAGG AGTCATACTG AAGACTTCAA TGTTTGCTAA AATCAGACTG AAAGCACTTA 120 CTGAAGTGAC CTCCCTGGAT AGGACCTTCA ACCTACCTGC TCTTCCTACA GGATTTTTCA 180 ACAGCTCAGC TGACATTGCT GGATGATGTT TAACAGACAC CATGGATCTT GAATTACAGA 240 TGTCCTCATA AAGAGACCTG ATTGTTTCAG ACATTAGGAG ATAATGTCAT TCTAGCAACT 300 CAGCTTAATT ATTGTCATGA CTGGACTTAC TCTTATCTTA GGTGGTGGAG AGATTTTATC 360 CTGAGATTTG GCTACCCTCT ACACCTCAAA CATGAGGCTA ATTTTAGATT AAAAGAAAAC 420 AAAAAGTGAA TACTTTGAAG ATATTGGCCA ATTTCACCTG TTAACTCTTT AGTCTTAGTC 480 TCTGCTTTTG GAGTATGAAT GTCAAAAGTA ACCATGCACA GATTTCAAAA ATACTTTAGT 540 TTTTTTTGTT TTGTTTTGTT TTGTTTTTCC CCAAAAGTTA AAGAAAAACT TCACTGCGAT 600 GCTGGCAAAA AAGAAACAGT ATTACTAAAT ATCAAGTCTT AAAAAGAAAT AGGGGAACTG 660 AATCTACTGA CAGACATTAT CAAAACATTT GTCCTCCAGG AAGGGAGCCA GTCAAGACTA 720 TTTGGTAACA GTGTGCTTGT GATTTCTGCA AGTTGGTTTC ACATTTCTGT TTTACTAAAG 780 ATGTGTCTCA CACAGTATTC CCTCCAACAG GAGGCAGTCC ACCCAAGAGG GGCAGCCAGG 840 AGTGGGAAAT AAGTAAAACA GTAGAAAGTT ACTTTTAAAT TATTTCCAAG GTTGTGAAAA 900 CATCTCATAG TTCCACTAAA CATGTATTGC CTCTTCAATG GGTTTCTGGA ATTTTCTTGG 960 CCTAAAACCT TTTGCAACAT TTAACATATC AGCTTGTGCT AGCTGCTTCT CTCTACCCTT 1020 CTTTGCCCTA CTGCAAACAA AAGAATTCAT TTCATTCAAC AGATGTTTTT CGAGCACCTA 1080 TTATTAGGCA GGTGCTGTGA CATGGAACTG GGGAAAAAAA GACAGTATGT TCAGAACACA 1140 ACTCTTAAGG GTATCTCGAT TTATTAACCA AAAACAGTAG TCCACTGCCA TTCCATCTGA 1200 CTTAACCTCA CTTCATATAT TTTTGTTTGT TTGAAGAGTC GGAGTCTTAC TCTGTCTGTC 1260 ACCCAGGCTT AAATGCAGTG ACGTGATCAT GGCTCACTAC AGCCTCAAAC TCCTGGGCTC 1320 AAGCAATCCT CCTGCCTCAG CCTCCAAGTA GCTGCGCATG TCACCACGCC TGGCATTTTT 1380 TTTTTTTTTT TTTTGAACTT TTTTGTAGAG ATGAAGTCTA CGTTGCTCAG GCTGGTCTGG 1440 AACTCCTGGG 1450
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