| Tag | Content |
|---|
EnhancerAtlas ID | HS187-25084 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr9:100150500-100151840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr9:100151329-100151343 | TGCTTCCTCTTTTG | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 100150534 | 100151704 | | chr9 | 100151128 | 100151479 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH09I097388 | chr9 | 100150688 | 100151650 |
| Enhancer Sequence | GGTGGCCACC CTGAAGGTCC CCTCCTGCCA GGGTCGAGGG CAAGGTCAGT GAGGATATCC 60
TCTTCACCCC TTTATTCTCC CAGCCCCCTG ACCCTGGGGC CCTGGACACC TGGCCAGATC 120
AGCTGGTACT AGTACTACTG CCACCACTTC TGGGGCGCTT TGATTCCAGC TTCACTCCCT 180
TGGCCTCCCT GAACCTGTGT GTTTCCTCCT CTGGGAAAGT GCGGCAGGAA CTCCACCTGC 240
CTCACAGGCT CTCCTGAGCA CCTGGTTCCT AGCACTCACA GCATTGTTCC TGCCATCACA 300
CCCCTCCCCC AGGGCAGAGC CAGGCACAAA GCCCTCCACA TTCCTCTCCA TTGTCACCAT 360
GTGAGTCCTG CACCACAGGG CCATCATCCC TCCACTTTTC AGATGAGAAA ACAGAGGCCA 420
AAGAGGAGAG TGACTTGCCC AGGGCCCCAT AGGAGAGGCC AGCTTCCTCC TCCTAGCTGG 480
AGGCCCCATC CCAGCTGCCT TCACCATGCC CCTCAGCACC ACTGCTGACC AGGGTCCCAT 540
CCTCTGGGCT CTCGATGTGT GTCCAGGCCC CCAGCCAGGC CCAGCCGTGG TGGGAGAAGA 600
CAGGGTAGTC CCAGGAGGCC CAAATGAGTG GCTCCTGCCT GCCTCAGCCA CAGGATTCTC 660
TGCCCCAAAG GCTGGGCTGA GGCCATGCAA AGGCTCCACC TCCCCAGGGA AACCCCCAGG 720
AAGTTCCCCT GCACAGAACA CTTTCTTCCT CCACTCAGGA AGGGGGACTC CGAGGTGCTA 780
TCTCTAATTG ACAGGCTAGG GGTGCCCAGG GTGATGGGTG AGGCCACTTT GCTTCCTCTT 840
TTGTGTGGAT GCTTGTGAAA TCCTCTCAGG AAGTAGCCAC CGGGGATCCA TTAGTCCCCA 900
TATACTCCTC ATAAACCATC TGGGATATGT GTCATTGCAA ATGAGGCATC AGGGCCGGAA 960
TCTGTGACTG ATCAGCAGTG CCTGCTATGG TGCCAGAGAG GGCAGTTGCA GAGTGCACAT 1020
ACCTGTCCTC TACTCTAGCC ATTTGGACCC ATGGCTGGGC AGCCTTTTTG ACTACCTGGC 1080
CTATGGGATT CCTCGGCAGT GCCCATCCCT GGTGCAGGCA GGGAGCCCCC TCCCCTTGGA 1140
GCTGCAGTCC AGACAGAAGA GCAGCTGGAG GCCAGCTTCC TGAGGACCCT CTACCTTCCC 1200
CATCTGCCAA CAGCCTGGAG GGGGCTACCA GCCAGTGCGA TGGGCCAGCC AGGGACCCAA 1260
GCCAGGGACC TGCTCAATCT GCCACCTCAT CAAGCCCTCC TGGCTCAGCA CAGCACAGCC 1320
ACCACTATGA CCCATTGCTG 1340
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