| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02178 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:47942960-47944700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr1:47943320-47943337 | GCAAGTCCCGCCCTCTT | + | 6.38 | | ZNF263 | MA0528.1 | chr1:47944509-47944530 | CCCCTCCCCTCCTCTTGCTCC | - | 6.88 | | ZNF263 | MA0528.1 | chr1:47944515-47944536 | CCCTCCTCTTGCTCCTCCTCT | - | 7.82 | | ZNF263 | MA0528.1 | chr1:47944512-47944533 | CTCCCCTCCTCTTGCTCCTCC | - | 8.37 |
|
| | 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 |
| GH01I047477 | chr1 | 47942901 | 47944366 |
|
Enhancer Sequence | CTAGGGGCCA CCTGCATTCC TTGGCTTGTG GCCCCTGCAT CTCTCCAATC TCTGCTTCTA 60
TCATCACATC TCCTGGTCTC ACTGTGACCT TCCTGCCTCC CTCTTATAGG GACCCTTGTG 120
ATTACACTGG GCCCACCCTG ATAATCCATG ATAATCTCTC CATCTGAGAT CCTTCATTTA 180
ATCACATCTG CAAAGTCCCT TTCACCATGT AAGGTAACAT ATTCACAGAC TCTGAGGATG 240
AGGATGTGGA CATCTTGAGG GTGGGGAGCA TTATTCGGCC TCCCACACCA TCTTGCAGAT 300
GAGAAAACTA AGACTTACAA AGGTCAAGGA ACTTGCCTAA AGTTCTACAG CCAGTAACTG 360
GCAAGTCCCG CCCTCTTTGG ATTTGAGCCT CCAGCTCTTA ACCTCAAACA AGAAGACTGC 420
TGGTGCAGGT GAACCTTGAA CTAGGTTTTG AAGAATGAAT CAGAGTTAAA AAAAGGTGTG 480
TCCAGTGGAG GAATGGTGTA TGCAAAAGCA AGCTGAGCAC TGGGTGTGCT TTGGTACCAT 540
AAAATGCTCA GATTCGCTGG GGGTGCAGGG AGGTGAGACA AGACAGGTAG GCAGGGTCTG 600
GATGGTGGAA AGCCGCCTAG AGCAGGCTAC AATGTTTGCA GTTGAATTGA AAGATGTGAA 660
AAACCATTGG AGGATTTCAC CTGTATGTCC TGGGTAATCC CTTCCCCTTT CTGACCCTCA 720
GTTTCCAGCT CCTCTGCCCT GATCTGCTTT TTCCCTCCCC ACTGTCCCTT TGTCCCCTCC 780
CTTCTCACCC CCTTGCTGCC AGGCCTGGTC CCATCCATCC CTGGGCAGGA ATGAGGGCTG 840
GGTGAACTGC CCCCTTCCCC CATCCCCAGG ACAGCGACGG TTTCCAAATA TCTGTCTGTT 900
GAAATAATGT TCTCTGGGCA CTGGGCCTCC CTCCCTCCCT CACATTCCTG GGCGAGCCGG 960
CCTGTTTGGC TTGCTCGGAC AAATATTGAC TTTCTCTGTC CTTCTCACTC TGGGTCTGTT 1020
TAAAAGGCAT CAATCTTTGC CGGGGTGTGA GCTCCCTCTC CGTAACCTGT GGCCTCTGCG 1080
GTCCTATTCG GGCAGGGAGT GGTAGGGGAG GGGCTCACAG GCTCTGGGGA TACCCCTTTC 1140
TTGCTTGGCT GCACTATAGA GGCTTTTGGT GCAATGCTGT TCCTTGTCAG CTGCTTTCCA 1200
CGCGGTCCTG CGTGGGGCCT AACAGCCCAC TTATGGAGCC TCTACTTGAG GGTCAGGTCT 1260
ATGCCCGTGG CATGTGCACT GAGACCTTCA TACACATTTC TCTAGACTCC TCAATAACCA 1320
GGCAGGAAAC CCTGCTGATT CTACCCTCAA ACAATTATTC ATCATCCAAC CACTTCTCAG 1380
CCTCCACCGC TACCCTCCAG GTCCCAGACA CCATCATCTC CTGGATCTGA CTCCTGGATT 1440
ATTAAGTTAA CTTCCTAAAT TCTGCCCCAC TTCCCTTCAG TCTGTTGTCA ATTTTGGAGC 1500
CAGAGGGATG GGTGAACATG TTGGTTAGCC TGGCTTAGAC CCCCCAGCTC CCCTCCCCTC 1560
CTCTTGCTCC TCCTCTCTCC CTTTGGGCCT CAGGGTTTTT CCTCCCACCT GAAAAACTTT 1620
GCACGAAACT GTTCTCTCTG CCTGGAACGG TCTTCCCAGA TCTGGTAGAT TCCCTCCCTT 1680
ACCTCTTAGT AAAATGTTTC TCTGGCCGGG CGTGGTGGCT CACGCGTGTA ATCCCAGCAC 1740
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