| Tag | Content |
|---|
EnhancerAtlas ID | HS077-01689 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr11:9385290-9386720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr11:9385932-9385947 | CGCTGAGTCATGGTG | - | 6.43 | | TCF7L2 | MA0523.1 | chr11:9386372-9386386 | GAAGATCAAAGGCA | + | 7.31 |
|
| | 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 |
| GH11I009361 | chr11 | 9382592 | 9387533 |
|
Enhancer Sequence | GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCA GGAGGAACCC AGGAGGGGGA 60
GGTTGCGGTG AGCCGAGATC GCGCCAGCCT CGTGACAGAG GGAGACTCCG TCTCAAAAAA 120
AAAAAAAAAA AAAAAAAGGA AAGAAAGAGA AAATACAAAC AAAAGCTGAG ATTTGCTGAG 180
TTCCTACCAT GTGCTACGCA ATGCCAACAA CAAGGTGGCA TGGAATAATC CTCATGTCTG 240
TTAAGTGGGT GGGGGTAGGA GTGGGGGTAG GAGTAGGGGA GTGTCACACA TCTGCAAACG 300
GTAACGTTGA ACTTCCAAAG TAGGTCCATC GGGCTCTCAG GACCCGCGGC TGTCCGAGGC 360
CTCAGTTGCC TCAATTAGTC TTAGGCTAAC TTCCTCCTTG CGCTGGGGGG TGGGGAATAC 420
TTTCCCGTGC GGAGGCCTCA GCTCCTCAAT GTACAGAGAA GAGCCTTGCA GGGCCTAAAC 480
ACTGGAGTTC AGGGATCCTT TATCAAGCTG CCAAACCTTT TCAGGGGCTT GGAAGGACAC 540
CTAAGGGCGG AAGCGGGCGC GTTGTGGCCC CCGTGGGGCA GTGGGAAGGC AGCAGGGCCT 600
CGCGGGCGGA GGCCGGAGCG CCGCTGACGC CGGAGCGGAA GCCGCTGAGT CATGGTGGGG 660
GCAGGAATGC AGCGCATTTG GAGAAGGCCC GGGACGCCGG CGGCTCCAGC ATTACTGAGC 720
AGTGACTTGG CGTCCGCACC TTCACTGCAG TCGGGAACCA CCAGTGACGG CGGTGACCGG 780
AAGAGCTGAG TCACCGCAGG CGACGGCGAG CGACGCCGGC GGGGAGGGGC TGACGCGCCT 840
GGGGCCGCGC GCCTGGGCTC CAGGGCCCCG CGCGTCGCCA CGATCCCGAC GTTGCAATCC 900
CCGCCAGCTC GGCGGGGGCC GCACGGGGCT GGGTCTCCCG GATCCCGCCC GGGGATTGGA 960
GTCTGAGGCT GAAATTTGAA ATCTTGAAGT GGCCCCAAGC CACAAATACT ACAGACTGGT 1020
TTCAGTGGGA ATTAGGACCT TGTGAAAGGA GACAGCAGTG CCCCAAAGAC TGGGTAGATT 1080
TTGAAGATCA AAGGCACTTG CCTAGGAACA AAAATGATTT GCCTGACTCA GTTCCAAAAT 1140
GCAGCAAATA ATAATTAAAG CGAAACACAC ACGCACTGTT TTTTTTAAAT GCAAGAGCAA 1200
AACTTTTAAA ATTCCAAAAG AAAATAAATC TTGGTTTCCG AGATGAATTC GTCAAAGGAA 1260
AATATCTTGG GGCCCCCATA TCACTAAGCT AAAGGGAAAA GTCAAGCTGG GAACTGCGTA 1320
GGGAAAACCT GTCTCCCATT CTATTCAAAG TTACCCCTCT GCTCACTAAC ATAAATGCGT 1380
TATCTGATTG CCTCTTTTGG AGGCTGGGTG CGGTGGCTCA CACCTGTAAT 1430
|
