| Tag | Content |
|---|
EnhancerAtlas ID | HS050-62912 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr7:73037010-73038520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:73037320-73037341 | TGGGGAGGGAGGGAGAAGGGA | + | 6.03 | | ZNF263 | MA0528.1 | chr7:73038280-73038301 | GGAAGAGGGAATGGGGGAGGA | + | 6.32 | | Zfx | MA0146.2 | chr7:73037767-73037781 | CGGGGCGCGGCCTG | + | 6.43 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACACAGTCC TCTCTACCCC AGCTATCTCT GACTGGGGTT ACATCAGCCT TGAGTCAGCC 60
TCTGGGTGGG GGGGCAATTT TGGGGGTGCG CTCTGTCCCT TACCTTGCCA GCTCCCCAGA 120
ACCTCTCCTC TTTGGTCACC CATCGTCAGG GTTGGAAGTG AGGCCCCCTC CCAAATAGAG 180
TGATGTGTAG TATATAATGA GCAGCCAAAG TTGGGGTTGG GTGGGAAATG GGAGACCCTT 240
AGGAGGAGGA GTGCCGGCAT CCGGTGTACC AGGACCTTAG ATGCCCTGTC CCAGGCAGTC 300
GCGTGACATT TGGGGAGGGA GGGAGAAGGG ACGGGAATTT GAACTTTCCA CACGGGTCCG 360
ACGCCCTGGC CGATCGGGTT GCAACATGAC CTGGGCCAGG GGCCAGAGCT TGTGGGCCAA 420
GGTTACTCCG CCTCCAGCCA ATGGGGTCGC AGCTGGGCGG CTGCGGTTGG GGGCAGGCAA 480
CACTCCCCTC ACAGTCCCCA CCCCAGCTCC TGCTCCCCCG CAGGGCGGCA GGTGCCGATC 540
TGTAGCCAGC GGTTCTCAGA AGGGGAGGAG GCGCCGCGGA GGAAGAGGAA TATTTGCACA 600
GAGAAAAGAT CAAGGCCGGC CGATCCCCCT TTCTCCCCTA CGGGTTTTCG GTTGATAATT 660
TATACTGGCC CCTCAACTCC GGGGAACTTT GCTCCAGGGC ACTGGGCCAG GCCTCGGGTT 720
CGCGCCCTCC TCTGGGACGC GGGGCGTGGA GCGGCAGCGG GGCGCGGCCT GTGCGCTCTC 780
GGTGGCACTA AGCGGGGGTC CCAGGCAGCG ACGGGCGCTC AGCCTAGTGT GGCGACGTGG 840
GTAGGCGAAC CCAGGCCTCC CGGGCACCGG CGTAACCTCT GCGAGCTGCG CCTCTTGGAC 900
ATTTCTGGGA CATCCTCCTC CCGCCACCCT TAATGTAGCA GATCAAGAAG AGGTGTCTCA 960
GCAATTGCGG GGAGGTGGAC GTGAGAGTGG GCCAGTTCCA GTCCACTTTG GTTATGAACT 1020
GGGACAATCA GGGGCGCTGG GAGTATCTCA GGGTCCAGGA ATAGGGCGGG CTTGGGCCGG 1080
GGCTGCTGGG GAGAAGGCCG AGGCCTGCAG GGGGTCGGGT GGAGTGGCTC CAGAGTGGAG 1140
AGTGGGGATG GGCGCGGGTG GCCTAGGGAC CAGGGGCGCC TGGCATTTTT GTAGGGACGG 1200
AGGGGCTGGG ACCAGAGAGA GGGGACCAGA GGTCCAGGTA GAGGTGGGGC GCAGGCGGTC 1260
TGCGCTTCGG GGAAGAGGGA ATGGGGGAGG AATGGGAATC AGAAATGCGT GGGTCCGTCA 1320
GGGGCCAGCG GGCTGGGCCG CTGTAGGAGG ACCTCGGGGC TGGGAGAAAG GGGGTGTCCA 1380
GGGCGTGATC GGAGCCTCCG GGAGCCGCAG GACCGGGCTC GGGTGGGGTG TTGAGGGCCC 1440
CAGCGCGCAG TCCTGCCCCG GACCCCCCCC CCATCCCCAC CTGGAAGCCA AGGCCGTCAG 1500
GGCCCGGAAC 1510
|
