Tag | Content |
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EnhancerAtlas ID | HS048-03167 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:204694670-204696000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr1:204695212-204695227 | GGACGTGGGTGGTCA | - | 6.31 | JUN | MA0488.1 | chr1:204695886-204695899 | ATGACATCATTGA | - | 6 | JUND(var.2) | MA0492.1 | chr1:204695885-204695900 | TATGACATCATTGAA | - | 6.19 |
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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 |
GH01I204726 | chr1 | 204695741 | 204695890 |
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Enhancer Sequence | GACAGAGACC AAATCCGTAT TTCTTATTGC ATCAGGATAA AACACCTGGG TTTGAATCCA 60 ACACCATCAC CTATTAGCAT CACCTATTTG CTCCTGTCAT TTTCTCTTTC TGGCCTCAGT 120 TTACATGTTT GTAAAATGAA GTTCTGGATA TGATGACCTC TTGGGTTCCC TCCAAAGATG 180 ACTTTCCAAG AGTCTGCTGT TTTACATGCT ACCAAACGGA AGTGGAGATC TAAAATTTCA 240 TGTGCTCACG GAGTGGGCCA CTCCCACAAT GCCATCTCCC CTCCCCTTGT GTGACTGTCT 300 CTGGTGGTCT GCTCCTGAAA GAGTACACAA AGTCAGGATG CAAAGTCCTC TCACTGGAGA 360 ATGAAGACAC CGTTCATTCT GGTGTTTGTT CTGCGGAGCT TCCCAGAGCT GTAGTCAGTC 420 ACCTCACCCC GGTGCCAAAC ACTTGATGTG CTGACTACTC CCGTGCTCTT AATAAGCTTA 480 TAGTCCGGAG AGATGATTGA AGGGCTGGGA GAAGAGGGCT GTGGAGGGAC AGGACCAGCT 540 GAGGACGTGG GTGGTCAGAC TCCTAGATTA ACAAAGCCTA CAGATGCCTG TTGACAGAAG 600 GGAAGGAGAC AGGTTCTCAC TGATAGGAAG ACAGCAGCAA TGCAGGTACG ACTCATGTGT 660 CCATTTCCTG TCATCTGCAG GTGCTTGGTG AGACAGTGTC ACCGTTCTGG GAAGAGCTAG 720 TCTGGGAGAA GGAGTCAGGA TACTAGACCT GTCTGTGAGG CACTGGATGA CTCCAGGTGA 780 GTCATTCACC TTCCCCCCGA CTCCAACCCT CCCAAATCTT GGTGTTCTCA TCTTTATGGA 840 CCTAGGTTCT TTGACACCTC ATTAATCTGA AGGTGGAACC AAAGAATGCA CACCATAGAA 900 ATGGCTACAT CAAAGACTTC ATCCCCAAAT ACATCTCTTC TGGTTCAAAA GCTTCTTGGA 960 ACACAAGCAG ACCTGACCCT CCTCCTCTTC TGCACCCCAT GATGTCCACC CCCTGCCCTC 1020 TGTCATTCTT CACTCTCTAC TCTACTTGCC TTCTCTCTCC CTTGTGAATC TCTTGTAAAT 1080 GGAAGTCCTG GTCCCAGCAG CGTGCTGGTA AATGTTTAAC AAACAGCTTT GAGACTGGGG 1140 GGAATGCCTG ATTTGTAGGG CTTGCCAACT GCCAATTGTA AATACTCCTG CCATGACTAA 1200 TTTCAAGATA CCAAATATGA CATCATTGAA TGCAGAGCCA GGAAAAGAGT CACAGTAGCA 1260 CACTGATGTA TAGTATTTTC ACCATACACA TAGAACAGGA GTAAATGACC TCAAGAACAC 1320 AGATAATATA 1330
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