| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04712 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:168862050-168863480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:168862417-168862428 | AGCTGTGATTT | - | 6.14 | | RARA(var.2) | MA0730.1 | chr1:168862184-168862201 | GGGTCATGTAAGGGTCT | + | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 168862190 | 168863079 | | chr1 | 168863241 | 168863304 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I168892 | chr1 | 168861982 | 168863769 |
|
Enhancer Sequence | TCAGCTCAGC ATTGGCTTGT AACTCTTCTC TGTATTTCTG TGCATAGGTA GTCCATATTA 60
TTCACCCTCC TTTGTGCAGG GTCCATTTCA TCCATCCAAA TATCCCAAGG ATCTGGGATA 120
TTTGCAGATT CCCTGGGTCA TGTAAGGGTC TACTCTGACA TCATCTCATG TTATTCTACA 180
GCTTGAGTCT GTCTCCATGT GTTACTTCTG TCTGGCCAGT GATCTCTCAG TGTGTTTTTG 240
ATTCCTCAGT GTTTATATCA TCTCTAGTGA TTAAAATTTT AACATAGCAC AACACAGCAT 300
AGACACGGCA CCTCTTTTCC TATGATGCAG CTCAGCAACA TAGCATGATT CATCTTCCAT 360
GTAGAACAGC TGTGATTTGT GCTTCGTTGA TGTCTGCCTC CCTACTTTTC CTCATAGCTC 420
TCCTCTCATC TCCCCCATTT AGCATCTTTC ACCGTTACAA GCAATGATCA GATAAACAGA 480
GAGATGAAGG TAGTACAAAA GAAATCTCAG CCCTATCCTC CCTGTGGCTA TGTTGGATCA 540
ATTTTCAGCC CATCTTCCCT AGTCCCTTCT CTGCTGGACT TAATGTTCCC TTCCTCCTGC 600
CAGCTTAATC CTATCCAGGT CCTGAGTCAG TACTGACTAC AGCTGCCTTA GTTCCAGCAG 660
GCTCCAACTG GTTCTGGAGT TGGTCTGGGA TATGATCATC TTTTATTTCT GACTCAATGT 720
AAGACTCAGC TTGGGTATGT ACTCCTCTGT ATTAGAGCTC CCAGGATGGC TTGATGCCAT 780
TCTCGTGTGC TGCAGTGGCA CCGTCTGCTT GCCTCTGTTA TTATATACTT CCCGCTTGAT 840
TCCAACTGCC TGGTGACAAG GCAGCCTTCC CCACTGGAGA TGAGAGCTCC AGGAGGTCAG 900
GGGCTAGCTC ATCATCCATG TATCCCTGGC AATTTACACA GTCCCTGGAG CCTGGCCCAA 960
GCCTCCCTGT TTCTACTCTT GTTTTCCTAC AACATACTCC TCACACAGCA GCCATGATGA 1020
TCATTTAGAA ACATAAATCA TCCTTTCCCT GTAATTTACC AGTTTTCAGA GCAAGGGGTT 1080
GGTGCCCTAC TTTTCTGAAA TGGTATTTGT TGTGTTTTTG TTTTGGCTGG TGGTTTTGTG 1140
GTTCTCTAGC AGTTTTTATT TTTTGTCTGT GTTATTATGA ACTAATAGGC TTAAAATATA 1200
TTCAATATGA GATAGTCAAT TTCAGTCACT ATTGTTTTTG ATGTAAAGAT TGTCCCATCT 1260
TGCACCGGCA GAAGTTCTTT CAAACTAGTT CCTGGGAGAT CTTTTTGACA CAGCCCTGTT 1320
ATCTTTGAGA GATTCTTTAT TGCCACCGCA AGGTTTATCA TCAGGTTCAT CTTACTTATT 1380
TCACCCTGGA CTTGGACTCA GCCCTTCTCC ATGAATCTCT GGTCCCTTTT 1430
|
