| Tag | Content |
|---|
EnhancerAtlas ID | HS095-28036 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:73037130-73038520 |
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 | ACCTCTCCTC TTTGGTCACC CATCGTCAGG GTTGGAAGTG AGGCCCCCTC CCAAATAGAG 60
TGATGTGTAG TATATAATGA GCAGCCAAAG TTGGGGTTGG GTGGGAAATG GGAGACCCTT 120
AGGAGGAGGA GTGCCGGCAT CCGGTGTACC AGGACCTTAG ATGCCCTGTC CCAGGCAGTC 180
GCGTGACATT TGGGGAGGGA GGGAGAAGGG ACGGGAATTT GAACTTTCCA CACGGGTCCG 240
ACGCCCTGGC CGATCGGGTT GCAACATGAC CTGGGCCAGG GGCCAGAGCT TGTGGGCCAA 300
GGTTACTCCG CCTCCAGCCA ATGGGGTCGC AGCTGGGCGG CTGCGGTTGG GGGCAGGCAA 360
CACTCCCCTC ACAGTCCCCA CCCCAGCTCC TGCTCCCCCG CAGGGCGGCA GGTGCCGATC 420
TGTAGCCAGC GGTTCTCAGA AGGGGAGGAG GCGCCGCGGA GGAAGAGGAA TATTTGCACA 480
GAGAAAAGAT CAAGGCCGGC CGATCCCCCT TTCTCCCCTA CGGGTTTTCG GTTGATAATT 540
TATACTGGCC CCTCAACTCC GGGGAACTTT GCTCCAGGGC ACTGGGCCAG GCCTCGGGTT 600
CGCGCCCTCC TCTGGGACGC GGGGCGTGGA GCGGCAGCGG GGCGCGGCCT GTGCGCTCTC 660
GGTGGCACTA AGCGGGGGTC CCAGGCAGCG ACGGGCGCTC AGCCTAGTGT GGCGACGTGG 720
GTAGGCGAAC CCAGGCCTCC CGGGCACCGG CGTAACCTCT GCGAGCTGCG CCTCTTGGAC 780
ATTTCTGGGA CATCCTCCTC CCGCCACCCT TAATGTAGCA GATCAAGAAG AGGTGTCTCA 840
GCAATTGCGG GGAGGTGGAC GTGAGAGTGG GCCAGTTCCA GTCCACTTTG GTTATGAACT 900
GGGACAATCA GGGGCGCTGG GAGTATCTCA GGGTCCAGGA ATAGGGCGGG CTTGGGCCGG 960
GGCTGCTGGG GAGAAGGCCG AGGCCTGCAG GGGGTCGGGT GGAGTGGCTC CAGAGTGGAG 1020
AGTGGGGATG GGCGCGGGTG GCCTAGGGAC CAGGGGCGCC TGGCATTTTT GTAGGGACGG 1080
AGGGGCTGGG ACCAGAGAGA GGGGACCAGA GGTCCAGGTA GAGGTGGGGC GCAGGCGGTC 1140
TGCGCTTCGG GGAAGAGGGA ATGGGGGAGG AATGGGAATC AGAAATGCGT GGGTCCGTCA 1200
GGGGCCAGCG GGCTGGGCCG CTGTAGGAGG ACCTCGGGGC TGGGAGAAAG GGGGTGTCCA 1260
GGGCGTGATC GGAGCCTCCG GGAGCCGCAG GACCGGGCTC GGGTGGGGTG TTGAGGGCCC 1320
CAGCGCGCAG TCCTGCCCCG GACCCCCCCC CCATCCCCAC CTGGAAGCCA AGGCCGTCAG 1380
GGCCCGGAAC 1390
|
