| Tag | Content |
|---|
EnhancerAtlas ID | HS187-09914 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:402990-404060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr17:403086-403097 | TGTGGATTGGG | - | 6.14 | | Foxd3 | MA0041.1 | chr17:403729-403741 | GTTTGTTTGTTT | + | 6.32 | | Nkx3-2 | MA0122.3 | chr17:403344-403357 | ACAACCACTTAAC | + | 6.02 | | TCF3 | MA0522.2 | chr17:403693-403703 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH17I000499 | chr17 | 402563 | 404293 |
|
Enhancer Sequence | CTTTTCTTTT CTCATCTGCT GGGCAAAATC CACTTTCTTT CTTTTTAGGT GGAAAAAAAA 60
TGTTTATGTC CAGATGCCCG GTCCCTGTGA TGATAGTGTG GATTGGGTGC AAAAATGCTT 120
CAGCATTTTG GTTCTTAACA TTTAAAGGCA GATTTTTAGA ATAAGAAAAC AAACCAAAAC 180
AGCATTCCAA CATTCTTACA TTGATAGCAC GGATTCCAAG ACTTTTGTCT CTACTGCAGA 240
ATTACAAAAG TCTGCACAAG AATTCAAGCA ATTATCTCGA TACCATCTGC ACCTGAGCGC 300
AGTGCATAGA CGAGGCCCCA CCTGCTGCTG CGGAAAGGGG CAAAGAATAG AAAAACAACC 360
ACTTAACAGC AAAATGTGAC TTCGCTACCT ATCCAAAGGA TGATCATTGA TGTCCTGAGA 420
GAACCAAGAA ATCACGCACT GGAGGACCCC TGACCGGGAG GAAAGGCAGG GGTCTTTACT 480
CAGTAGATCT TGAATAAGAA CACTCTCTTG CAAGACACAG TTGGGTCACA GCTGGCCTTG 540
TGCAATGAAA ACCAAAGGGG AACTTCTGCT TACTGGGTTT CTACAGATAG AGATGAAACT 600
ACATCCTCTC TCTCAAGAAA CAGGAAAAGC CACGCAGGAT GAGTGAGGAT GTGCGGTGGG 660
TACCCACACA CCCACCATGG GGATGTGCAG CAAAACCAAC TGCAGCAGGT GTTTTGGCAA 720
GAGCTAGCGG GCTTTTTTTG TTTGTTTGTT TTTTGAGACA GAGTCTCGCA CTGTTGCCCA 780
GGCTGGAGTG CAGTGGCACG ATCTTGGCTC ACTGCAAGCT CCGCCTCCCA GGTTCCAGCG 840
ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGGTTACAGG CGCCGGCCAC CACGCCCAGC 900
TAATTTTTTG TATTTTTAGC AGAGACAGGG TTTCACTGTG TTAGCCAGGA TGGTCTTGAT 960
CTCCTGACCT TGTGATCCGC CCGTCTCGGC CTCCCAAAGT GCTGGGATTA AAGGCATGAG 1020
CCACCACGCC CGGCCAGCTA GCGACATTTT AAATGTACAC CTCCTTTAAT 1070
|
