| Tag | Content |
|---|
EnhancerAtlas ID | HS148-02001 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr10:12374880-12376450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr10:12376160-12376175 | TACTTCCTGGGAAAT | + | 6.25 |
| | | 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 |
| GH10I012332 | chr10 | 12374649 | 12377076 |
| Enhancer Sequence | TATTTAGGAC CTGGCAATGT TTGTCCCCCA GGGTAAGGGG TAGGGTATCT TTAAAGGTGA 60
CAATTGGTAT CCTTATATAC AGGGGAGACT TTATCTCAGC TTTTATATCC ATACAATAGA 120
GTTTTATGTC TGGGCATGGT GGCTCATGTC TGTAATCCCA GCACTTTGGG AGGCCGAGGT 180
GGGTGGATCA CCTGAGTTCA AGAGTTCGAG ACTAGCCTAC CCAACATGGC AAAACCCCGT 240
CTGTACTAAA AAAATACAAA AATTAGCTGG GCGGAGTCTG CAGTGAGCCA AGATCGCGTC 300
ATTGCACTCC AGCCTGAGGG ACAGAGTGAG ACTTTATCTC AAAAAAAAAA AAAAAAAAAA 360
AAAAAAAAAA CTGAGATAAA ATCTCCCCTG TGTGTAAGGA TACCAATTGA AATTAGCAAC 420
CAAAGCCAAA ATTGGTGTAT TTTGTTTTTC TGAGTGTACA AAACTTGGGA TTAGAGGTTG 480
GAAAATAAAA GATGTGAAAC TACCCTTGGC TAGCATCCAT CTGCCCCTTC TCTCAACCCT 540
GCGTCATTTG TCACTTGCAG GGAAGGTGGA GAGAAGGACG AGATGGCAGA TGGAGGAAGA 600
GAGGACTCAG AAACCCTCGT TTCTTCTGGT TTGCTTCTGA CTTGAACTGA AGCTCATGCC 660
TCCTTGAACC TGGGAACAGT TTGATTTCTG GAAGGAGCTG CGTGCAGAAG CTCCTTTAAA 720
ACTTTGGGAT CAAATTAAAA CTTTGGGTTT TAGGTAGGCA CAGCCACAAA AAAGTTGAAG 780
CTGGCATGTC TTGTGCAAGG CTACCTATCA AGACAGAAAT AGAAGTGGAT CTCTGGCCTG 840
GCCGTCTGGG ACTGCGATGT CTCATTGTGG GGCCTGCCTG TAACTGAAGG TTCCGCATGA 900
GTCACGGACT TCCCTGGTGC AGGGCAGCAA CCCAGGGGCT TGGTAACTGG GTTGAGGGAA 960
AGAGAGAAGT TTTTGTTTAT GATCTCATTC CAATCAGAAT GTGTCCAGAC GCCCAAATAT 1020
TTGATTTGAG CCTGGTTGCT AAGAGACCTC CCACTGGGAC CCAGCTGCCT GCGGGCAGGA 1080
AGGCGGTATT GGCATCATTT CAGATTTCTG CCAATTTATT TTGAAACCAG AAAACCTAGA 1140
ACCTCGGCCT CCTCAAGGCA ACCAGGGGGA GAGGAGAGAT CTGAGTCAGC CAAACTAGAG 1200
AGAGAAAACC CCCGCTAACC TTCTGCCAGG GAGCTGTAGG AAGGTTCGGG ATAGAATAGA 1260
ATGATGACAT TGTGCTTGTT TACTTCCTGG GAAATAGGCC GGTAGGGTAA TGAAGAAGAA 1320
GTTGGAGTTC TGTGCTTAGA AATGCAAGTG TCATCTTGAA GAAACCTCAG GGATTCCAGA 1380
ACAATGCTGG ATTTCCGGGT AATAATTGGG CGTTGTGAAG GCTGCCCTGA TTGGATCCAC 1440
ACACCCAGCA TCTTGGGTTT TAATTGCCCG GTGACTTAAA TGCCTTAGGG AAATGGCATG 1500
AGTAACATTG TCATAGGTGA GCGTGTGCGG GGTCGGTGCA CATGGGACAG GTGGGGAAAC 1560
CTGCTTCTGG 1570
|
| |
|
|
|
