| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00402 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:15790510-15791860 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr1:15791449-15791462 | TGTTAATTAATTA | - | 6.12 | | Nr2f6(var.2) | MA0728.1 | chr1:15790978-15790993 | TGACCTTATGACCAT | - | 6.02 | | RARA | MA0729.1 | chr1:15790975-15790993 | TAATGACCTTATGACCAT | - | 6.17 |
|
| | 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 |
| GH01I015462 | chr1 | 15789135 | 15792046 |
|
Enhancer Sequence | CACTCCAGCC TGGGGGACAG AGCGAGACTC CGCCTCAAAA ACAAAAGGCA TAATAATAGC 60
ACCTACATCA CAGAGTTGTC ACGAGGATTA AAGGAGATAA TCCATAGGAA GCCCAGAATG 120
GGGTAGGTGC TGTGTTAGTT GTTGTCACTG TCCCTATGAT GGAGAGAAAG TTACAGAGAC 180
CATGTGACAT CTTCTGTGTG GCCCAAGGCT AGAGTTCAGA ACAGCATTTT CCTCTGTGAC 240
CTGAGACCCC TGGAGCCCTC ATCAGACCCT CCATGCCCCA TAGCAAAAGC TGTCCCCTGT 300
GCCATTAGGT CTTGCTGCTC AGAACCTGAA TGAGGGCGGG TCTCCTTTGA CATAGACTCC 360
AAGGGTCAGA GATCCAATGA CAGTAGCCAC CAAGAGGAAC AGAGTTCCCG CCCTTCCCTT 420
GTGAAATCAC CAGAGGTTTG GAAGATTCTA GGAAGGGATG AGTAATAATG ACCTTATGAC 480
CATAATGAGA TTATGAGTGT TAATCACATT ATGACATTTT TTCCTAATGA CATAAACCCA 540
TAAGTATAAT GACATGTTTT TCCAGGGGTA CATCCACATA CGTACCCTCA AATAATTCCC 600
ATTGCCCTCT TGACTGGCTT ATCTGTAAAC ACAAGGACAC ATCAAATCCT GCGGTGAGCG 660
GTGGTGGAAG AGGCATTTCA TGCTTATTAA GATACAAGCA CAACCTCCTG TTTGTTTCCC 720
CAGACAACCC TGGGGCAGGC GCATTTCATC TGAGACAGTG AGAGTGGGGA GGCCTCCAAA 780
TGCTTGGCTT TTCGGCCCAG CTCTGTCAGT CACGGTGAAA CCTTGGGCAA GCCACTTCCG 840
AACCTCAGTT TCCTCATCTG TAAAATGGAA ACACTGTTGG TGAAGACTAA AAGAGGTGAA 900
AGGTGAAAAT GCATCATACA TTGCAAAATG TTATGCAAGT GTTAATTAAT TACTTATTAG 960
TGGTCTTAAG CCAGACACTT AACTTCCCTT TTTTTTTTTT TTTTTTTTTT TTTTGAGACA 1020
GAATCTTACT CTGTTACCCT GGCTGGAATG CAGTGGTGCA ATCTCGGCTC ACTGCAACCT 1080
CTGCCTCCCG AGCTCAAGCG ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG GCATTATAGG 1140
CGAGTGCCAC CATGCCCGGG TAATTTTTGT ATTTTAGTAG AGGTGGGGTT TCACCATGTT 1200
GGCCAGGCTG GTCTCAAACT CTTGACCTCA AGTGATCTGC CCACCTTGGC CTCCCTAAGC 1260
GCTGGGATTA GAGGGTGAGC ACCGCGCCCG ACCGACACTT AACTTCCCTA GGCTTCAATC 1320
GGAAGTGAAG AATTGTGTTA ATCTCATCCT 1350
|
