Tag | Content |
---|
EnhancerAtlas ID | HS182-18610 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr6:25332370-25333840 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:25332819-25332837 | GGAAGAAGGGAAGGACAG | + | 6.4 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH06I025332 | chr6 | 25332828 | 25333428 | GH06I025333 | chr6 | 25333629 | 25333828 |
| Enhancer Sequence | GTATTTGCCT TTTGACTTTT GTTGCCAGGA GCCTCAAATC TAAAGATAGG TCATAATAGT 60 CATAAAAGTA GTGATGAACT GGAAATCTGC TGTTTTTGTC TTTCCAGCCT AGGAGCCTTT 120 TCCCCATTTA CTCGTTTGTT TACAAATATT TTTTGAGTGG TTGTCATGTG CTGGGCACTG 180 AGAAAGCTGT AGTGAATAAG ATGGGTAGGC AAAAATGGAA GTGGTTCGAT TGTGCTCATC 240 CAGGTATGAG ATAATAGTGG CTTGGGTGAG TGTTTGCAGT GAAGGTGTAG AGAAGTGGGT 300 GAGTTCTGAA TGTATTTTTA AGGTAGAAGC AAGTGAATTT GCTGATGATC AAAAGTGGGG 360 AATGAGGGAA AAAGAAGAAT CCAGGACGAT TCCCAGGTTT TGATTAGGTA TGTGATACTG 420 ACTTTTGCTG AAACTGAGGG ACATGTTGAG GAAGAAGGGA AGGACAGCTG AAAACATTTG 480 GGAAATGTTA ATTTGTAATA CTTGTTACAT ATCCAAATGG AGATGTCATT TAGTTTTCCA 540 GAGCTCAGGG TAGAGATTCT GTCTCCATTC CATAGCACCA CCCACCATGC AAACATGCAT 600 ACACACACAC ACACACACAC ACACACACAC GCGCACACAC ACACACACAC TTCTTTTAGG 660 GAACTTCTCA TGTCCACAGC AACCATGTGA TTCTACTATG GTTTCAGCTT CTTCAGCCAC 720 AAAAGACCTG ATACTTCCGT GCCTGCTGGC CTTTGTGCTA TAGTCTCCTG GCCACAGTGA 780 TTAGTCCAGG GGGTGGACAT ATGACCCAAG AGTCCTTCAT TGGGGTCTAG GGAAATACCG 840 CCTTGAAGAG AGAGGCTCTC TTTTTCTGCT GGAGAGACTA AATGGTTTAC ACTCAGATGT 900 GATTCCTGCT ACGTGGAGGA AGTCCATCTG AATAGTACAG ATTGATGACC TTGCCCAGAA 960 AAGCAGAGAT TCTACAGAAA TGTGGAAAGT CCCCTCCCTG CTGTTTACTA CACTGTATCC 1020 CTTGGAATGC CAGCGCTTAA AGGTGTTAAG TGAGTAAAAC TTCTTTGGTC AAATAAATTT 1080 AAAGAAAGAA ATTTCTTGAC AGCAGAACTT TTCAGATGAG CCTTTGTAAT GAATATGCGG 1140 CTGGGCATAG TGGCTCATGT CTGTTATCCC AGCACTTTGG GAGGCTGAGG TGGGTGGATT 1200 GCTTGACCCC AGGAGTTCGA GACCAGCCTG GGCAACATCA CAAGACCCCT TCTCTGCAAA 1260 AAATACAAAA AATACAGAAA AATCAGTGAT GAGTGCAGCT GTAGTCCCTG CTACTTGGGA 1320 GGCTGAGGCA GGGGCATCGC TTGAGCCTGG AAGGTCGAGG CTCCTGTGAG CCAAGATTGT 1380 GCCACTGCGC TCCAGCCTGA GTGACAGAGC AAGACACTGT GTAAATAAAT AAAAATATGT 1440 TTTGTGCTTC TTTAAGAGGA GGATTAGTAA 1470
|
| |
|
|
|