| Tag | Content |
|---|
EnhancerAtlas ID | HS101-31538 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:184091370-184092860 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:184091799-184091814 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGAGAAAGA GATGGAAGAG AGAAGCGCAC TGCCTCAAAG GGCACACTAA AAGCGGGTGG 60
GGAGCCTTAG GAGTAGCCAG CAGAGTGAAT CATACAGGCT GAGAACTGGA CAGGACCAAG 120
GTCCCACCCA GGGCAGGAAT TCCTTCACAG TCTCCCGACA GCTGGTCATC AGCCTCTGCT 180
TCAAAAACTC CCGTGTCCTC TAGTCCAGCC TGGTCTTACA CTTGGTTTCA GTGAGAAGAG 240
CTCCTTTTTT CTTACGTTGC TGAAATCTGC CCTGTTACAG CTTTTACCTC TTGGTTCTAG 300
TGCTGCAAAT TTACTCTTTC TGCTGCAAAA CCTTAGGATC ATTTGATTTT TAAACTGAAT 360
GAAGGCTGGG TGCAGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC TGAGGCAGGT 420
GGATCACCTG AGGTCAGGAG TTCAAGATCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT 480
ACCAAAAATA CAAAAATTAG CTGGGCATGG TGGTGGGCAC CTGTAATCCC AGCTACTTGG 540
GAGACTGAGG CAGGAGAATC GCTTGAATCC GGGAGGCTGA GGTTGCAGTG AGTTGAGATC 600
ATGCCACTGC ACTCCAGCCT GGGGGATAGA GTGAGACTCC GTCTCAAATA ATAATAATAA 660
ATAAACTAAA TGTAGGTATG AGACTCTACC ATAATGATCA TAAGGATGAA AAGAAAGGAC 720
TAGAAGGGAC CCATAGGAAC TGCCCTTCTT CCCTGACTCA GTCCTGAAGG AAGAAGGGAC 780
GCTAGGGTTC TTGAGGATAG ATTTTAGTTT TTTAAACTAT TGCCCATAAA ACATGCTTCT 840
AGTCTCTTTC TGTTCAGGCT GCTGCTTTCT AGACACATGT TAGTTTAATA TGGTCCCTCT 900
TAATAAATTA GCATATGTCT TCAGGGGGAT GTCCGGTGTT CAGGCCAGTA TATTTAAGTG 960
TAGTCCACTC GGAATAGAGT TCTGTACGAG CATTTCCACA ATGGGGATGC TAAACATCAA 1020
ACAGACAAGA ATTACTAGCT TTAAGAATAG CAGCTTCAGT AATGTTACAT GGTAAGTTTG 1080
GGGGCAATTT AATTCTCTCA GATCCTTTTC GTAGGAAGTG CTAGGGCCAG AGGCTTAAAT 1140
GATGGAAGCA GGGCATTGTG GCCTGAAAGC TGGAATAGGA CTTTACTCAT TAATTTACAC 1200
ATGTAGAATT TTTTTTTCTT TTTGAGACGG AGTTTTGCTC TTGTCACCCA GGCTGGAGTG 1260
CATTGGCATG ATCTCAGCTC ACTACAACCT CCACCTCCTG GGTTCAAGGG ATTCTCCTGC 1320
TTCAGCCTTC CAAGTAGCTG GGATTACAGG CATGCACTAC CATGCCCGGC TAATTCTGTA 1380
TTCTTAGTAG AGACGGGGTT TCGCCATGTT GGCCAGGCTG CTCTCAAACT CCTGCCCTCA 1440
GGTGATCTGC CTGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG 1490
|
