| Tag | Content |
|---|
EnhancerAtlas ID | HS149-00198 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr11:9385340-9386810 |
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 | AGGAGGGGGA GGTTGCGGTG AGCCGAGATC GCGCCAGCCT CGTGACAGAG GGAGACTCCG 60
TCTCAAAAAA AAAAAAAAAA AAAAAAAGGA AAGAAAGAGA AAATACAAAC AAAAGCTGAG 120
ATTTGCTGAG TTCCTACCAT GTGCTACGCA ATGCCAACAA CAAGGTGGCA TGGAATAATC 180
CTCATGTCTG TTAAGTGGGT GGGGGTAGGA GTGGGGGTAG GAGTAGGGGA GTGTCACACA 240
TCTGCAAACG GTAACGTTGA ACTTCCAAAG TAGGTCCATC GGGCTCTCAG GACCCGCGGC 300
TGTCCGAGGC CTCAGTTGCC TCAATTAGTC TTAGGCTAAC TTCCTCCTTG CGCTGGGGGG 360
TGGGGAATAC TTTCCCGTGC GGAGGCCTCA GCTCCTCAAT GTACAGAGAA GAGCCTTGCA 420
GGGCCTAAAC ACTGGAGTTC AGGGATCCTT TATCAAGCTG CCAAACCTTT TCAGGGGCTT 480
GGAAGGACAC CTAAGGGCGG AAGCGGGCGC GTTGTGGCCC CCGTGGGGCA GTGGGAAGGC 540
AGCAGGGCCT CGCGGGCGGA GGCCGGAGCG CCGCTGACGC CGGAGCGGAA GCCGCTGAGT 600
CATGGTGGGG GCAGGAATGC AGCGCATTTG GAGAAGGCCC GGGACGCCGG CGGCTCCAGC 660
ATTACTGAGC AGTGACTTGG CGTCCGCACC TTCACTGCAG TCGGGAACCA CCAGTGACGG 720
CGGTGACCGG AAGAGCTGAG TCACCGCAGG CGACGGCGAG CGACGCCGGC GGGGAGGGGC 780
TGACGCGCCT GGGGCCGCGC GCCTGGGCTC CAGGGCCCCG CGCGTCGCCA CGATCCCGAC 840
GTTGCAATCC CCGCCAGCTC GGCGGGGGCC GCACGGGGCT GGGTCTCCCG GATCCCGCCC 900
GGGGATTGGA GTCTGAGGCT GAAATTTGAA ATCTTGAAGT GGCCCCAAGC CACAAATACT 960
ACAGACTGGT TTCAGTGGGA ATTAGGACCT TGTGAAAGGA GACAGCAGTG CCCCAAAGAC 1020
TGGGTAGATT TTGAAGATCA AAGGCACTTG CCTAGGAACA AAAATGATTT GCCTGACTCA 1080
GTTCCAAAAT GCAGCAAATA ATAATTAAAG CGAAACACAC ACGCACTGTT TTTTTTAAAT 1140
GCAAGAGCAA AACTTTTAAA ATTCCAAAAG AAAATAAATC TTGGTTTCCG AGATGAATTC 1200
GTCAAAGGAA AATATCTTGG GGCCCCCATA TCACTAAGCT AAAGGGAAAA GTCAAGCTGG 1260
GAACTGCGTA GGGAAAACCT GTCTCCCATT CTATTCAAAG TTACCCCTCT GCTCACTAAC 1320
ATAAATGCGT TATCTGATTG CCTCTTTTGG AGGCTGGGTG CGGTGGCTCA CACCTGTAAT 1380
CCCAGCACTT TGGGAAGGAG AGGCGGGCGG ATCACTTGAG GTTAGGAGTT CCAGACCAGC 1440
CTGGCCAACA TAACGAAATC CCGTCTCTAC 1470
|
