| Tag | Content |
|---|
EnhancerAtlas ID | HS147-13165 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr13:100752230-100753440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr13:100753032-100753046 | TACTTCTTCTTTTT | - | 6.19 |
|
| | 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 |
| GH13I100098 | chr13 | 100750631 | 100754083 |
|
Enhancer Sequence | AATTCCCAAG TGGTTCTGGT ATAATTTTAA GAAAGAAGGT GACAGTTACA TATTTGGATT 60
TAGTTTTCAT GTAAAACCTT ACATTTTTTG GCACTTTACT GTTTATAAAA ACTCATTTGA 120
TCCTTTTAAT AACTCCCTAG GAAATCAGGG AGGTGTCATC ACCTACATTT TGTAGATGGA 180
AACGGGGGCC CAGAGAAATG ATTAGCTCAA TGACTCACAG CTGAGAGTTG ACCCAAGTCT 240
TGTGACTCTG AGGGTCAATG CCACTTCCTA TGTGCCAAGC CATTTTCAGG CATTTCTTTT 300
CTATGTGTGG AAAATACAGG AAATCATTAT TCCTGTGGGA GAGAACCAGT GGCAATATGT 360
TACTGGGGAG TCATTTTGCA CACGCTGACC TCTCTCATTT TGGCTGTGAT TGGCTAGCCT 420
TTATAAACAG AATTGATTAA AGTTCTTTCT CAGAACCTTT GTTGCTAGGA AATACCTTAC 480
AAAGAATTTT GGACTGGGCG TGTAGCCAGT TTGTTACATG CTTAACAAAA ACAACAAACG 540
TTAAAATTCT GTGTAGAGGT CCAAATTAGC AGACTTCTTC AAACGTTTTC CTTCATTTAG 600
AAAATAAACT TTATGTTGTG GCTTTACACA AATGGTCTGA GTGTTGACCT GATTCTTCAT 660
TTTTGACCTT CCATGAATGT CTCCCAGGAG GAAACAGGAA CAGAGCCTTT ATGGGGCTCA 720
TTCCAAACCA GTTCAGACTT GTCGTGGGAA TGGTTCACAT TGGTAGTTGT TCTGTTATAG 780
TTGTGTTTGC TTGTACGAGT TCTACTTCTT CTTTTTTTTT TTTTTGTTGA GACAGTGTTT 840
CGCTCTTTTT GCCCAGGCTG GAGTGCAACG GTACAAACTT GGCTCACTGC AACCTCGGCT 900
CACTGCAACC TCCGCCTCCC GGGTTCAAGC GATTCTCCTG CCTCAGCCAT CCGAGTAGCT 960
GGGATTACGG GCATGCACCA CCATGCCCAG CTAATTTTGT ATTTTTAGTA GAGATGGGGT 1020
TTCTCCATGT TGGTCAGGCT GGTCTCGAAC TCCCAACCTC AAGTGATCTG CCCGCCTCAG 1080
CCTCCCAAAG TGTTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCGAG TTCTACTTCT 1140
AGTTACTGGG TAACCGGGAG GCATCTATGC TTTTTACAGC TTTAGGCCAC ATTATTACAA 1200
GTTCACATGT 1210
|
