| Tag | Content |
|---|
EnhancerAtlas ID | HS187-23012 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr7:106765820-106767460 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:106767137-106767158 | AATGACTTTCTGTTTTGTTTT | + | 6.15 |
| | | 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 |
| GH07I107125 | chr7 | 106765904 | 106768046 |
| Enhancer Sequence | TGTATTTATG CTATGTTTGT TTAACAAATA AAATTTTTAT CTGAAATCAG GAATGAATTT 60
TAATGAAAAC CAAAGTGGCC TCTAGTACAC TAAAATCACA CTTTGGGTGT ATTGCTGAGG 120
CCTCAGTGAT CCAGAGAGAG ATCCCTTAGG TGGGATCATG CTAAGCCCCA GAGGAAAAAT 180
GTAGGAGAGC ATCTTCAGAG CAGGTGGCTG CAGTACAGAG GAGCTGGAGT GTCAGAGACC 240
ACACCCGCTT TCTGGCTGTT TACTTTCCCC AGTGAAGAGG GATTTTACCG ACGAGGTTAA 300
TTACAGAGAG TGGACTCTGA GTGCTGAGGA GTAATGGCAG GGTGAGGGAA AAGGGAAACA 360
GGAGGAGAGC AGTAGACCAT AGTGATGGAG GTGGGGCTGA GAAAAAAAAT ACTACTTAGA 420
AATGGTGATT GGGCTGGGTG CAGCGGCTCA TGCCTGTAAT CTTAGCAGTT TGGGAGGCCA 480
AGGCGGGTGG ATCATGAGGT CAGGAGTTTG AGACCAGCCT GGCCAAGATG GTGAAACCCT 540
GTCTCTAATA AAAATACAAA AATTAGCTGG GCACAGTGGC AGGCACTTGT AATCCCAGCT 600
ACTCAGGAGG CTGAGGCAGG AGAGTCGCTT GAACCCAGGA GGCAAAGGTT GTAGGGAACC 660
GAGTGCACCA CCACTGCACT TTAGCCTGGG TGACAGAGCA AGACTGTGTC TTAAAAAAAA 720
AAAAAAAAAA AAAAGAGGCC AGGCGCGCTG GCTCACGCCT GTAATCCCAG TACTTTGGGA 780
GGCTGAACTG GGCAAATCAC GAGGTCAGGA CATCAAGACC ATCCTGGCTA ACATGGTGAA 840
AACCCGTCTC TACTAAAAAT ACAAAATACA AAATACAAAA AAAAAAAAAA AAAACCAAAG 900
CCAGGCGTGG TGGCAGGCAC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATG 960
GCGTGAACCC GGGAGGCGGA GATTGCAGTG AGCTGAGATC GCACCACTAC ACTCCAGCCT 1020
GGGCAACAGA GTGAGAATCT GTCTCAAAAA AAAAAAAAAA AAAAAAAAGT CGTCATTGGT 1080
ACGAGAGGTA GCAGGAAGAA GAGAGAAGAG GAAAAAGCTG GATTTCTGTG TGAAGGCTTA 1140
TAGGAATTGA ATGGGTTGGA GAGAAAGACA TAAAGTTGAC CAGAGCGAAG CAGGTGCACG 1200
ATACTGATGC CTGATGCACT CTCCTCTCCC CCCTTTCCTT TCTGAGAACA GCTTCTCAGC 1260
AGGCAGACAT CTCGGTTGCT TTGGTTTGAA GTTCTAGATG GATTTTGTGA AGTGAGAAAT 1320
GACTTTCTGT TTTGTTTTAG TGTGTTAGCC TTCCTTATTT GAAGTAGGAG GAAGTGAAGT 1380
TTGGTTGGTG TGGTTTGGTT AATACCTGAA TTTTAAAGGT TTCTTATGCA GCAGTGAATG 1440
AGAAGTCCCT GGGATCTACT TTGTCTGTGT TTGTGTGTCA TCTTAGAATC TAGTTTGAGA 1500
TGAATATTGG GCAGATAGTA AACAAAGGTT TACATCTACC TTACCCTTAG AGGGGAAAGT 1560
GCAGTGACCC TTTCTCTTAC TAGCTAGTAG TTCTTTCATG TAGTCTTTAC ATAATGCAAA 1620
TAAATGGTAT ATATATCAAT 1640
|
| |
|
|
|
