Tag | Content |
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EnhancerAtlas ID | HS038-21284 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:61875630-61877380 |
Target genes | |
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) |
ZNF263 | MA0528.1 | chr8:61876698-61876719 | GGGGGTGGGGAGGGAAGAAGG | + | 6.26 |
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| Number: 2 | ID | Chromosome | Start | End |
GH08I060963 | chr8 | 61876014 | 61877059 | GH08I060964 | chr8 | 61877351 | 61878192 |
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Enhancer Sequence | TGTATTTGGA AAAGCTCTGG CAATGAAAAT ACTCCTGAGG GGGAGGATGC TAATTTTAAG 60 GAGCAAATGT TAGTAAACTG ACGGAGTCAG TCATCCCCCT GACTACGTGG AGATCAGTGA 120 GGAATATAGG ACTCGTTGCT CCTGGTCTGT AAATGTGGAA CAAAACCCAT TCTTAAGAGT 180 GGGATCTTAG TCTTCTTGGG GTGAGAGGCA AATGCTTGGC TATAATGAGC AAAAGAGCTG 240 GGGTCATTAT TTTGATAGTG TGTTTGCTGC CTACTTTTAG TCATGCACCT GAGACATTCT 300 TATTAGCAAG CTTGGAGCAG CAGTGGAGTG TTGAAAAAAT TTCTCTCAAA CCTGGGCTCT 360 AGGACAGTCC TCCTGCACAC AGATGAATGC CCCTGTGAGC AAATTGCCTC CCCGGCCTGT 420 TCAGAGTCAC CTACGCTGCT GGCAAATGGT TTTTCAGAGC AAGGTAAGCC CTGCAGAGAC 480 CCAGAGGCCT GTATATTTAA ACAATTACGG CCTGTGTGTG TCTCAGCCTC CTGCTGCATG 540 CTCCTGAGCA AGATGGTGTA ATATGTGCAT TTTACATATC AATAGCAGAG GAGGCTGTTT 600 CCAGATGGCT GTACCTATTT CAAAGCCACC TTTTTATGCA GAAGGAAGAC TGTGTGACCT 660 CCCTCCAAGT AAATGTGTTT TGTAAGTCCT GGGAATGAAT GCTTAAAAAA TGGTCGTGGG 720 CTATATTTCA TGTCCAGTCC AACATGTTGT GTGTGCACAG CTGTTCGGGG CTGGCATGTG 780 GTAGCATAAT AAAAGGAAGA TTACCATTTC CAATTTTTTC CCCTTCTGAA AGCTTGATAT 840 GCATATATGA AACTTGTGGA AAAAAATATG CATAATGAGA CAGGGATGCT GGGTCTCAAG 900 GCACTAGTCG GTGCACATCT GGAGTTTCTA GCATTCTAGA GATAGTTACT TATTCCCAGG 960 AGCCGCTGCC GGAGTGGGAA TGGTAGCCCG GTATCCATGG TGAGCTTCCC TATCTCACCG 1020 TGCCAGGTGT GCGTGTGTGT GTTATTTCTT GGAAAGGCTG TCCTCTGAGG GGGTGGGGAG 1080 GGAAGAAGGC AAGAGAGGAG AGGAGGAAAA AAACAGAAGG GAGGTAATTA GGCGCCACCT 1140 TGCCCAATGG AGCCTGCTCA GGTGTCTGAA ATCAAGGATG GGGATTGGAA GGGTGCTGAT 1200 GGAGTCTGAT GATTCCTCCT GCCTGCCAAG TCCACGCTTG TTTCTATGGG TACAAGACCA 1260 GGGGAAAGAA ACCCTGGGGT CAGAAAAGAG GCATGGATCA CAATACCAAG CAGGATGGGC 1320 CTTGCTACTT GCCTCTTCTG CAATGTGGTA TTAGTCTTGA ACTGACAACC TGAATTCATG 1380 CTGATTTTTT CCCCCAGTTT AGACATTGGA AGTGTTTCAA ACTTCGTAGG CTGTTATTTA 1440 GGAAAAGCCT TCATGGGATA GCATTTTTTT TTTTTTTTTT TTTTGAGATG GAGTCTCTCT 1500 CTTTCGCCCA GGCTGGAGTG CAGTGGTGCG ATCTCAGCTC ACTGCAAGCT CCGCCTCCCG 1560 GGTTCACGCC ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG TGACTACAGG CACCTGCCAC 1620 CACACCGGGC TAATTTTTTT TTTTTTTTGT ATTTTTAGTA GAGACGGGGT TTCACCGTGT 1680 TAGCCAGAAC GGTCTTGATC TCCTGACCTC ATGATCTGCC CGCCTCGGTC TCCCAAAGTG 1740 CTGGGATTAC 1750
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