Tag | Content |
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EnhancerAtlas ID | HS176-39132 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:8965560-8967700 |
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) |
MYB | MA0100.3 | chr8:8966604-8966614 | GACAGTTGGT | - | 6.02 | SOX10 | MA0442.2 | chr8:8967044-8967055 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr8:8967045-8967055 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27764 | chr8:8965682-8967092 | Fetal_Intestine | SE_28660 | chr8:8965442-8967304 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 8965991 | 8966124 | chr8 | 8966447 | 8966966 | chr8 | 8966486 | 8966781 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I009108 | chr8 | 8965552 | 8967023 |
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Enhancer Sequence | TAAATTTGAA TCCTTCATCC ATGCAAGGTA TAGGCTTAGA GTTCCAATTT TTCAAGAGAG 60 ACTTTATCTC TCCACCCAGA AACAGAAAAA CTTTCTTGTA ATACCTTGGT ACTGACGGGT 120 AGATTTTTCT AGTTGATCTT ATAACCAAGG AGGCAGCTCT AGCAGGGTTC CAGCTTAATG 180 CAGGAATTTC AGTTACCAGC TCCATGGTTT TATCAGGCTC AAAGCCTTGC TGAGGTTAAC 240 ATGTAGTCTC AATGTTGGCT TTAAGACGCA ATGCTACATA GATCCCTAGT GGGGGCCCTG 300 AACCAGCAGC CACAGAAGCA GCATGTTGTG GGCTGTCAGA AATAGACCCT TAGTCCCCAC 360 TGCAGAATCA GAATTTTTAT CTTAGCAAGA CTTATAGATG ACTCCTGTGT ACATTACAGT 420 TTGAGAAGCA CCACCCGGGT CACATGTTTT TTAATGCTCA TTCTTCCAAC CTCTCCCCTA 480 GAGAAGTTAT AATGTCTCTC ATGTTTTTTC TGGGCTCTTT GTTTTAAACT TCTGTCTGCA 540 TTTTTGGAAA CAAGAGATGT AATTTTCTTT CTTGAGAGCT CATCTGTGCA TTGAAAAACA 600 TTTTTGTTGA AACCTTCTTA GTTGGCCATA TTGCCAGGCC TAGAAATCCA ATCCTACTCA 660 TTCTTCAAAG TTAAACTTTA AGCTTTTAGC AGTTTCCTAT GCTAGCCCCT ACCTTTGTGC 720 TTTGTAATAT AGACACTCAA CAAACTATTT GTAGCTTTTG CATTCAAATG ATGGATTAGA 780 AAAATGTTCT TTATAGTGAG GTGGTATCAT TTTTGCTTAG TTCTGCCCCT TCTATGGTAT 840 TCTCTTTTTT AACATAATAC CCTCTGTGTC CCACTATATA CTTTTTACAA AGCTGGCTCT 900 GGCTCAAGCC AAGGCCTCCT CTCTGGCACC ATGGAATTTC TGTAGTGAGA TAGGAAAAAT 960 CTATTGTGCT CTCAGAGTCA CAGACACTGA ACAGCACAGC AGGGGCCAGG TTATCAGTGG 1020 CCTCTTCTTC CAGAGTTCCT GTAGGACAGT TGGTTATCTC AGCCTGTGCC CAGTCAGCCT 1080 ACACGTGGGG GTCTGGGTAG TAAAAGCTGC AGAGAAAGCA GCTCTGTCCA GATTCATTTG 1140 ATTAACTAGA CAGGCACATC AACTATACAC CCGTTCATTG CATTGCAGTA TCCTGAAACT 1200 CAGGGGCACT TGAAGGGGAA GAGGAAGTAG CTCCTGCCTC TGGGGTGCTT GTAATCATAT 1260 GGTAGTGAGA CACCCATATC CAAAAGAATG AGAAGAAAAA TCCCAAGATG TTAGAGATGC 1320 AAGTGCCTCA TAGGGAGGTA GAAACTGTGT ACACAATGCT GAGAGAACAT CAAGTAAAGA 1380 GAAGCAACTC CATTGGTTGG GACAGAGCAA CATCATCCCT TGTTTCCTTA AATTGCCAGT 1440 AAATATTTAT CCTCTGCTTG CTTCTGCTTG GGGCCAAATC ATTCTCCTTT GTTTTAGAGA 1500 GAAGGAAGGA GCCCCTCTGT TCTCCCCTTC CTGGGAAATT CATCGCACCA ACAGCGGAGA 1560 TCTTGGCTTT TTACACTATT TTGGGGGCTC TGCTTGGCAT AAAATAATAC ATTCCCTGCC 1620 TGGGGCTAGG ACAGATTGCT GCTTTTCTCC CACCTCCTGT AGGGTACATC TGGCCAACCA 1680 TCCCGATCAT TGTTTGCAAA GCTTCTATTC AAACATGTAT ATTGTTTTAT GAATGGCAAA 1740 AGAGGAAGCC AACAATAACC TTAGGTCTTC ATCTGCTTCT TTCATCTGAA GGGCGGGATG 1800 ATTCTGTGAA GTTCCCCTCC AGCCAGTGTC CCATGCTCTC TGTTTCCTGG GAAGCCAAGA 1860 TCATCAAGAT CATAGTCTTC TTTTGCTCAC AGCACACCCA CTCCTGGAGT CCCAAACCCC 1920 ATTCCTTTCT AAATCCTACT ATTCTTAAAT ACTCTCTTTC CCTGGTGACT TTGTATCTGA 1980 ATGGATTATT TGAAACTTCA ATGGTGCCTT ATAGTGTTAG GAATTGTTTT TATGTCTTTC 2040 TGACTTACCT CCCCAAATAT ATTTTAAGCT ATTTGAAGGC AGAGGATTCA TAGCATGTGG 2100 CACAACGGCA GGCAAGGGCA AGTTCTCAAA GATCTCAAGA 2140
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