| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14712 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:75977180-75978320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr16:75978177-75978192 | TGACCTTTGTCCTCC | - | 6.14 | | Nr2f6 | MA0677.1 | chr16:75978177-75978191 | TGACCTTTGTCCTC | - | 6.35 | | Rxra | MA0512.2 | chr16:75978177-75978191 | TGACCTTTGTCCTC | - | 6.19 | | SOX10 | MA0442.2 | chr16:75978193-75978204 | TGCTTTGTTTT | - | 6.02 |
|
| | 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 |
| GH16I075943 | chr16 | 75977478 | 75980341 |
|
Enhancer Sequence | CAGAGTGATC AGAGCAGGGC ATAATATGAT CTGATTAACA TTTTTAAATT ATCACACAGA 60
TTGCTAGCAG GGATAACAGA CTCTTGGTGA AAAGAAGGAA GTGGGAAAAC CAGCTAGAAG 120
ACTGCTCCTG TCTCGTAGGT GTGACCTGGC AGTGGCCTGA ATTTGATCAG AGGGTGTTGG 180
ATTTGAAGAA TATTTTGGAG GATTTTTAAA CAAATCAGAT GATGAATGTG AGAGAAACAG 240
AAAAGTCAAG CCTTAAGCTT TGAGCTTGAG CAGCTATGTG AATGGTGTCC TCGTAATTAA 300
GACACTTCTG GAAGCCTGGG CAAGGAGCAG GTGTGCAGAG GAGGAAAAGT AATCGGGGGT 360
GGGGTGGGGA GGGATGTATT AAAGATCAAA GTTTTTGTTT TGAATGCATT AGTCTCATGT 420
TGCCCATTAG CTGTCCAAAT GGAGATGTCA GGTAGAATAT GAGATGCAGG GACAAGGCTG 480
GAGATCAGCA TCACTTAGGT GACCAGAGCA TTGGTAAAAG TTGTACACTG ACAGCTAAGA 540
GCACAGTCTC TGGAAGCCAG ACCATCTAGA TTCAAATCTC AACTCTACTC TTCACAGATT 600
GAACTTGATT GTCCTGGCCT TCTCATCTGA AAATTAAGGA TGAAACTAAA CATACCTAAT 660
TGAAGAGACA TGAAGATTAA ATTAGTTAAC ATATGTAAGC ACTTAGGATG ATGGCTGGAT 720
CCTAGAAAGT GTGATGTCAA TGTTATCTAT GATTACAATC AGAGTTCAGA GTTGTTTTTT 780
TTTGTTGTTT TTTTTTTTCT GGCCCATCAG ATCAATTGCT AAATGGAGAC AGGGGATTGG 840
GTATTGTTTC CCAAGCATAC CTACTTTGCA TGGATTTTGA TTGCTAGCCC AAAGAGGTCA 900
AACTGCAAAC AAAAATTGGG GCGAAGCAAT TTATTTTGCC GGGGCAGTGA GCACTTTCAG 960
AGCAATGAAA ACTGATAAAG CTCCACTCCC TTAAATATGA CCTTTGTCCT CCCTGCTTTG 1020
TTTTCTTTCT TGTGCTTGTC ACCTTCTCAC GTATCATCTA TGACGTGCTG ATTTATTTGT 1080
TTGCTTTCCA TCTCCTGAGC TCTACGTAAA AAAGCAGGGA TTTTTTACTT TCTTTCTTTT 1140
|
