| Tag | Content |
|---|
EnhancerAtlas ID | HS048-11511 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:64389420-64390850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr14:64390214-64390229 | ATTTAATCATTAATT | - | 6.76 |
|
| | 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 |
| GH14I063921 | chr14 | 64388640 | 64390965 |
|
Enhancer Sequence | TTGCCAGGCC CTTCTTATTC CCTGTTGTTT CAAGAGTAAG TCATACATGT AAATTGTCCG 60
ATCTATTTAG ACAAGTATTT CACAAAGTGA GATATGTGAA GCCCTGAATC AGAATCTCTG 120
GGAGTTGGGA TCCAGAAACC TGCACTTAAA CAATAACCCT GAGTAATTTG CTGGCATTCC 180
AAAATGTAAG AACCCTGGAT TTATAATCAC AGCACAGCTC TGTTTAGTGC AGTCTGGTTC 240
TTTTGCACTC AGAAGTCAGA GGTGCTTGGA CTGCTGCCCC AGTAGAAAGT GTTCAGGCTC 300
ACATACCTTG ATTTTTCAAA AGAAAAGTGT TCAGTTTTAT GTGGTAGTTA AAAGGTAGCA 360
AGGAGTAACA AATATGTGTT AAAATAAATG TAGTCATTTC TTTATTTCTT CATTCCGTAG 420
ATATTTATTG AGCAACTTAG ATGAATCAGA AGAGTGTGAG AAGGAGGAGA GACAAATAGC 480
ACCCAACTTC TAGACTTTTA TCAGTATTGT GGGCTTATTT TCATGTGCTA AAAATACAAG 540
ACTTGCTTAC GCAGAGAGCC GGGAGCTATG TTCCAGTGAG GGTGGAAACA AAAGCCTCAG 600
TATAAGACTG TCAGGTGTTT ACACAAGGGT GTGGTTTGCT CATGTGGCAA CACGAGGTTG 660
CTGGACTCCA CATGCTGAGG CTCAAAGTAG AAATCACTGA TCTTATGTCA CATATTTTCC 720
CAACAAACTA AGTACTTAAA TCTGTATGTT GATTGAGGAA AAATAACAAA CTCCTGCTCC 780
CTCCTTCCCT AGCCATTTAA TCATTAATTC AATAAATGTT TTCTAAATTC CTATAGCATG 840
AAAGCTCTGG GGTAGGTGCT GCAGGCAAAA TGAGGAGCAA ACTCAGACAT GGGTCATGTA 900
CTGTTGGAGC CCATAAGCTA ATGAGGAGGC AGAAGTTGAT CAAATAATCT TATAGATATT 960
AGCTAATATT TTATTAAGCT TTATTAAGAT ATAATTTGAC ATCAAATTCA CATACAATGC 1020
AATTCACCCA TTTAAAGCAT ATGATTTAGT AGTTTTCAGT ATACTCACAG AGTTGAGCAG 1080
TCATCACATT GGATTTTAGA ACTTTTTTTT TTTTTTGAGA CAGTGTCTCA CTGTCACCCA 1140
GGCTGGAGTG CAGTGGTGCC ATTTCAGCTC ACTGCAATCT CTGCCTCCTG GGCTCAAGCA 1200
ATCCTTTCAC TTCAGCTTCC TGAGTAGCCG GGACTACAGG TGTGTGCCAC CACACCTGGT 1260
TAATTTTTTG TTTTTTTTTA TTTTTGTAGA GACACGGTTT CACCATGTTG TCCAGGCTGG 1320
TCTTGAACTC CTGGGCTCAA GCAATCCACT CACCTCAGCC TCCCAAATGT TGGGATTACA 1380
GGCATCAGCC ACTGTGCCTG GTCAAAAAAA GTATTCTTTT CCTACTGACT 1430
|
