Tag | Content |
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EnhancerAtlas ID | HS007-11980 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:170909800-170910840 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr3:170909979-170909990 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr3:170909979-170909990 | TTCTTATCTGT | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I171191 | chr3 | 170909324 | 170911819 |
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Enhancer Sequence | AAAAATGAGG TTGACAGGAA AAGAAACAAA CCTAGATATC TGAATTCTCT TGTCAAAGAA 60 ATTCAGCATG AGAGTACAGA GGTCCAAAAA GACCCACATA TACATTTAGA GATATCAGAA 120 AACATAAACC ATGTTATAGA AGGGTTTGAG GCACTGGTTT AGGTCTTAAA AAATTGCCTT 180 TCTTATCTGT TCAGTTTGTC ACAGGGTAGG CATCAGGGGT TTAAATGTGT GGTTTTCACA 240 AAATTTATGT ACCCCATAAA TCCTTAAGAG AGGGACTGAA GATCCCTTTC CCTCTTTCAC 300 TACTGAAGTG GTTGAAAGCA GATACCAGAG CATGGAAGTG AGCCAAAAGT TCTTTTAATG 360 AGATCATACA ATGCATGGAG GTCACCTCCA AAACCTCTTG TGGCCAGAGA CCTTTGGGTG 420 ATCAAATGTC TCTTCCAGTG AGTCATGTCT GAAATGCTGG TATCATTTCG GAGAATATAC 480 TGGAAAAAGG AGGAAAGCCA TTGTTTCCAC ACATTGAGAA TGTGTGAAAG GTATTGAGAG 540 ATGCTCATGT GATGAAACAT CCCTGCTGCT TTTAGAACCA TGAAGATTAG ATCAAATGAC 600 TGATCCTCTG TAGGGTTCCC CAGCAGTGCA GAAAGGCATA TTGGGCAGAA CCAGCCCTAG 660 AGACCTGACA GGTTCTTGGC AGCCACTGAG TGGTCAGGAT GACTAAATAA TCCATTATGC 720 TCTATCTGAA TGAGCAAAAT TTTAAGTCAG AAATTCAAAG TAAGTTTGCA CAATGGCACA 780 TCAAAACAGA GATAAACGTC AGATGTGAAG GAAATCAGCA GCCAGGCCTC CTTGTTTCCC 840 CTCAAATTTT GTGTTATGTT CTGTTTAAGA ACACAAAACA TATAATTTAT ATTTTTGCCT 900 ATCCCAAGCC ATGGATGTAT GTGTTTTTTC TTAAGTGCTT TAATTTTTAT ATTTTTCCCA 960 TTTATATCTA TAACCCAGCT GGAATAAATT TTTGAATATG GTATGTAGCA GGTGTCAGGT 1020 TTCATGTTTT CTTATGGATA 1040
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