| Tag | Content |
|---|
EnhancerAtlas ID | HS148-13353 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr4:39503780-39505230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr4:39504242-39504252 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr4:39504242-39504252 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr4:39504242-39504252 | AATGGAAAAT | - | 6.02 | | TCF3 | MA0522.2 | chr4:39505080-39505090 | AACACCTGCT | + | 6.02 | | ZNF263 | MA0528.1 | chr4:39504193-39504214 | TACTCCACCTCCCCATCCTCC | - | 6.69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 39504217 | 39504365 | | chr4 | 39504422 | 39504573 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I039501 | chr4 | 39503031 | 39505327 |
|
Enhancer Sequence | ATGTGTCTAT GCCTTGCAAA TAACCTTTTA AAAATAACAT TCCTGAGTTT AGTCATGACT 60
GGGAAAAACA GTCATGTTGT TACTCACTAG GGAGGGGTGG AATAGAAGAG TCCCCAAGGT 120
CTTGGATGGA AGAGTTCACA GACAAGGATG CCATTTGATT CTTTCCACAA GTAAATCTCT 180
CATGAATGAG AAATGGGCAC TGAATTCTAA ATAAGGACCT TCAACAAGTT GGTGAGAGGT 240
TAAGAGAACC AGATCAGATA TTTTTGAATA GCAGATTAGG CCTTACTGAT ACCTCTCCAA 300
GATAGCTGGT GCTGAGATGT GCATAGCAAG CTGTCAAACA CTGCTGCTTT TCTGCTTGCT 360
TGGGCACTAC ATTGACAACA ACCCCCTGGC ATATTTTTTT ATTCTCCCTA ACTTACTCCA 420
CCTCCCCATC CTCCTATCCC CATATACATA CTGCTCTGAG GAAATGGAAA ATAGCTCCTT 480
ATTAATACCT TTGGGACTCC TTGGAGAACT GAAATAGATG TAACCTACAA AAACACTGTT 540
CTGGGTGGAG GCTTCTGTCA GCTTTCCAAA TGTTCCATAA TTGACAAACT GTTTTTTGTT 600
TTTTGAGGCA GGGTCTTGCT CTGTCACCCA GGCTGGCATG CAATGGCATG ATCTCAGCTC 660
ATTACAACCT CTGCCTGCTG GGCTCAAGCA ATCCTCCCAC GTCAGCCTCC CATGTGGCTG 720
GGATTACAGG CACAGGCCAC CAAGCCTGAC TAATTTTTAT TATTTTTTTT TCCCAAAACG 780
GAGTCTTGCT CTGTCACCCA GGCTGGAGTG CAGTGGTGTG ATCTTGGCTC ACTGCAACCT 840
CCGCCTCCCA GGTTTAAGCG ATTCTCCTGC CTCAGCCTCC AAAGTAGCTG GGATTACAGG 900
TGTGTGCCAC CACACCCAGC TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTTACAGTAT 960
TGTCCAGGCT GGTCTCGAAC TCCTGACCTT GTGATCCGCC CGCCTCAGCC TCCCAAAGTG 1020
CTGGGATTAT AGGCGTGAGC CACCGCGCCC AGCAATTTTT GTATTTGTTA ATAGACACGG 1080
GGTTTCACCA TGTTGGCTAG GCTGGTCTCG AACTCCTGGC CTTAAGTGGT CTACCTCCAC 1140
AGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAACCACTAT GCCTGGCCAG TTGACAAACT 1200
TTGAATCAGA AGAGGGCCAG TACCATTGAA ACTCCCATAT GTTTCATTCA GACCCCTCAC 1260
AGCACTGGCA CAGTGCTGAG TACTCAGAAG GTATAGGATG AACACCTGCT GATTGACCAA 1320
GACCTCTTTC TTTCTCTACC TTTAGATCGC AAATTTAGGG AGGAAGTAGA GAAGTAGAGT 1380
AGTCAGAAAA ATCCCATAGG GACTTCCTAA AGAACTGACA TGTTGCCCCA GAGTTACGTT 1440
ACTGCTAAAG 1450
|
