Tag | Content |
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EnhancerAtlas ID | HS180-50684 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chrX:13077460-13078840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chrX:13077995-13078006 | GATGAGTCACC | - | 6.32 | FOSL2 | MA0478.1 | chrX:13077996-13078007 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chrX:13077996-13078007 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chrX:13077995-13078006 | GATGAGTCACC | - | 6.62 | Nr2f6(var.2) | MA0728.1 | chrX:13078013-13078028 | AGGGTCAAGAGGTCA | + | 7.91 | RORA | MA0071.1 | chrX:13078415-13078425 | TGACCTTGAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 13078278 | 13078619 | chrX | 13077920 | 13078128 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI013059 | chrX | 13077380 | 13078978 |
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Enhancer Sequence | AAATACTCCT CAGAATCAGA GCAAGGGCTT CTTACCCCCT TGCAAGGGTG GCCCAATCAC 60 TGTCTGCTTT TGATTTGTGT ACTCTGTGCC CTCTGTGAAC AGTACTGCCA CTTGAAACCC 120 GATTCCCAGA GCAGTCCTTG GACCTCTTGT ATTAGCATTC TCCAGACTGT GAATTAAAAT 180 GGCAGTTTTC TGTTTCAACC CTAGACCTTC TGAATCTGAA TTTCTAAAAG TGGGGCCCAG 240 GAAACTGAAT TTTTATTAAC TATCCCGAGG GATCTGATGT ACACTGAAGT GTGGAACTGT 300 GACCTCATAT CCTAAACCCA CGTTCTCCAT TGCAAATCCT TCAGCATCCT TACCTTCTGT 360 CTTACCCACC CAGAAGACTC CCTTCCCAAA TATGCATCCT GCATGGTGTC ATTGCATTTG 420 CTTTCCTAGG GAGGGATGAA GATAAAATCT TGACATGTGC TTTGTGGTGA GGGGAGAAAG 480 CAGTTTTTAT CTGAGGCTGA AAGGTTATAT CTTGAGCCTC AGACAGAAAA CTTAGGATGA 540 GTCACCCAAG GAAAGGGTCA AGAGGTCAGC TAGCCTGATC TTATAGAGGG AGACAGTCTT 600 GTGAGTCTGA CTAAGTTAAA CCATGATCTT GGGTCAATAA ATATTTGCAG AATGAAACAG 660 ACAATTTACT GATATTGAAA TGGCCAGGCC ACTTGGATGA TCTCCCTGAG TACAGTGTCT 720 AACTTTGAGA TTTTATACAT TATAGTAAAA TAGTGGCCAG GCATAGTGGC TCACACCTGT 780 AATTTCAGCA CTTTGGGAGG TTGAAGTGGG AGGATTGCTT GAGCCCAGGA GTTGGAGACC 840 AGCCTGAGCA ACAAAGCAAG ATCCAGTCTG TAAATTTATA TGTGTGTGTG TATGTGTGTG 900 TGTGTATAAA ATAGCTTGGG CACTCTCCAA GCTGACTGGG ACTCGGCCTT GACTCTGACC 960 TTGATTGCTC TTATTCTATG AATAATTCCA AAAAGATTGA TTATCTGATT ACTCAGGCCA 1020 CTGCAAACAG GAAGCGCCTG ATTAGAAGCA ATTTGCAAGA GCAAGAGGAA TATGCAAACA 1080 CAGGCACAGT GAAAGAGGCA AAAATTGACA GAAATTTCTG GAAAATTTGC TTATGTGGAA 1140 CTTGTTATTC CTTGATGATG ACAAATGGAT AGGTGAGAAC AAAGATAGCT GTAAAAATCG 1200 AGCACTTCCA ACTTCAAGAC TTGACCTTAA GAATCTTCTA GTACTTAAAA AAAGTAGGCC 1260 ATTGTTGACA AGTATAACAC TGACTACTTT GGGATGGAGA AGTAGAGATG ATGAGAAGTG 1320 AAAAAGGCTT TACACAAGTC ATGGAATTGA GTCAGTAATG ATCTAGGGGG CTGGAACTAA 1380
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