| Tag | Content |
|---|
EnhancerAtlas ID | HS145-27834 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chrX:108604170-108605770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chrX:108605190-108605200 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chrX:108605189-108605200 | TTTCACACCTT | - | 6.62 |
|
| | 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 |
| GH0XI109362 | chrX | 108605389 | 108605613 |
|
Enhancer Sequence | ATTTGAAACT GACATGTTAA CTGGCTCTTA AATTAATGGT GCCTGGAGTT AATAGCTATA 60
CAACAAGGAT GATGAGCTTA AAAGGAAGTA AAGATTTGGA AATTCCACAG TTATTTGATT 120
TCTCATAGAT AATCCAGATA ATTTCAGCAC CCAAACTGCA AATAAAAACC CACTTTGGAG 180
ACAATTTATC TGGTTTGGCT GTTTCTCTGG ATCTGATTAA GAAGGTATTC GTCAGATCTC 240
CTTGCCATAT GTGTCAACCT TGCCTTGATT CCTTGGCTCT GACATGGGAT TGGAAGAGAA 300
GCAGAAAAGA AACTCCAAGT CTTGCCCATC TGGCACTACC TCTTTGACAC TGTGATTTAA 360
AATAAGACTG GAGAAACTTC CAAGCACATG CCAAGGACTG CCAGGCTATA TGAATACCCA 420
GCTGGTCTTC ATATAGCATG GAAGGATGCA GATTAGCCAA TGAGTTACTC CAGTGAATAA 480
CACCTTGGAC AGAATCTAGA AGATAGCCTA TTCCAAATTA TCTCATTGCA GTCAGTTAGG 540
TGGATGGTCT ATTAGGCCTC TGGTTAGTAG TCTGTCTCGC TGGTTAGCAT TCCATGTATT 600
AAATTATCCT TCTGAAACCT AAGCTTATCT CTATGTAACT GACCAGAGAG AGAAACAGGT 660
AGAACAGGTC AGAACTAAAG TTCTACTGAA GTTAATGTTT TCATTGCCTA CAGCTGACTT 720
TGAATACATT CAGTTTTCTC TTTCCCAAGA TAGATGACAC CACTCTGGTG AATGTCACAA 780
TTAAGTGAAT TAGCACTCAT TGATATAAAT ACAACATGGA ATTTTAAAAT CAGTTAACCT 840
AATACAATGA AAGCATTATT TAAAAAAGTT AATCTGAAAA GCTGTTATCG AGTAGATCTG 900
GCAGTTCTTA GTAGACACTT GTACTAATTG TGACTTTTCA CAGTCAAAAG ATTTGGGTCA 960
GAGGAAAAGG AAACTAGTTG GTCGATATGT GATCCTAAAG CTGATCCATA GATTGGCAAT 1020
TTCACACCTT TCTCCCATGG GGGAGGAGAA AGCTGAATAA ATATATTATT CACATAAATA 1080
AGTGAATAAT ATGCTTACTT CCTTGTAAAG TCTAAAGACT AAGTCCATTT AGAAAATATA 1140
CGTCAGGACA TTCTTAAGAG CGTAGACCAA ATAATGAAAA GTTGAGGTCT TTCCTTTCTA 1200
CTGATGTGAT ATAACTAACC AACTAAGCTC GTCCAAAAAA TAGTCTGTGT GGATTTTTCA 1260
ATCGAAGCCA AAGAGGAAGA GATAAAATGC AAGATCAAGG AGCAGACTAC AAATGATACT 1320
GTCACATGAA GACCTAATTA GTCACTAATG ATTCATCAGT TTCATAATGG AAACGGTTTG 1380
GAATATATGG AACTGAAATA CAGAAGTTAT TAAGGACACT TGGTGCATTT TCAATAGTGG 1440
ACACTCTGCT GACAGCCAGA GTTGGAATTT AACTATGCAC CTGAAACAGG GAGAAAGGAA 1500
GTTCTAGTCC CAGCTCTGCC ACTAGCAAGC TGTGCAAACT TTGAAAGGGT ACTTTCTTTT 1560
CTGGGATTAG TTTCCCAGTC TGTGAAATAA GAAGGTTGAA 1600
|
