Tag | Content |
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EnhancerAtlas ID | HS091-11092 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:121151190-121152820 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:121152096-121152116 | TTGTTGTTGTTGTTTTGTGG | - | 6.72 |
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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 |
GH12I120713 | chr12 | 121151781 | 121151990 |
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Enhancer Sequence | GTAGGCCTCT ACGTTGTGGT GACCACTAGA CAGTTTTGAG CCAAAGGTCT TTGAAACTCA 60 AATCTTTGTG TGCCACTGCA TCCTGTTTCT TGGACTCCAG TGTGTCCCAC TTCTGTGACC 120 TCTTCCCGTG GCCTGGTCTG CCAGGCATGG TGGTTTGAAG CTGCGTTCAG AGGCTGATGT 180 TTGTTGGATG TCTATTCTGT GCTGGTCACT GTGTTCCACG TCTTTGTGCA CATCAGTGTA 240 TGTAATCCTC ACACCTCTTT GAGGAATTAC TGTTATCTCT GTTTTACAGC GAAGGATCTG 300 AGGCCTACAA TTCCCAGGCG GCTCTTTCCT AAGGCCCTGT GCTGGTTCAT CTTACCATGT 360 TGCCTCCAGT TGGGAAAGGA ATCCTTGAAA TTAAACTATA ATGAGGAAAA CTCACCTGAG 420 CCTGGTGCCC TCTTGGAGGG TGATAGGGAG GATCCTGGTC CAGACATGAG GCAGTTTGAG 480 CCATCTTCTT GCTCTCTTTT ACATATTGCC TTGGAGTTCC CAGACCTAGT TTGGATTTTA 540 ATCTCAACCA TTTTCTGGAA GAACAGACCC AGGAACTCAA CTACTTGGGG TTCCTTAAAT 600 TAGCCTCCCA TAGCCGCTTC CTGTGCTTGT GATAAAGTGC CAGGCTGATC TGGACCACAG 660 AAGCCTTTGG AGCACCTCAC TGGAGGTTTA GCGCCCCCTG GAGTTAGTCA TTTGTTAGAA 720 CACTGGTACA GATACCCATA GTATCAGTGT GGTTTGTAAA CTTACTTTGC AGTGTTTCTC 780 ATCTGATTTG CTACTTAGAG CCTGCAAATT TGATAAGGCC CCGATTTCAC CCCTACCTGG 840 TGGTATTTAT GCTATCATAA TCTCATACTG ACCAAGGCAC CTAAAGGCTC AAGTTCATGG 900 GTAATTTTGT TGTTGTTGTT TTGTGGGTTT TTTTTTTGTG TTGTTTGTTT TGAGACACAG 960 TCTTGGTCTG TCACCCAGGC TGGCGTGCAG TGGCACAATC TTGGCTCACT GCAACCTCTG 1020 CCTCCTGGGT TCAAGAGCTT CTCCTGCCTC AGCCTCCCAA GTAGCTGAGA TTACAGGTGC 1080 CCACCACCAT GCCTAGCTAA TTTCTGTATT TTTAATAGAG ACGGGATTTC ACCATGTTGG 1140 TCAGGCTGGT GTCAGACGCC TGACCTTTGA TTCGCCTGCC TTGGTCTCCC AAAGTGCTGG 1200 GATTACAAGC GTGAGCCACC GCGCCTGGTT GCTTATGGGT AGTTTTTTAT TGGGATGGTC 1260 AGATCAAGAC CAGCTAGCTT CCTGGGTCTG TGGTGTTCTC ATCTCTAAGC CACATATCAC 1320 AGTACCTGGG ACATTGCAAG GACTCCAGGC CTACTACAGG TATGTGGATT TGGATTAGAC 1380 TCAAGAGTTG TCATTTCAAT ATAAGACGGA ACTGTTTCAA GAAGGTCAGC TGAAGATACT 1440 GTAAAGTATC TTGGTTTTCA GTCTCTCTAG TTTTTACATT TAAGGATCTT GATTCACTTG 1500 TAATATTCCC CACATTGAGG CTGGGTGCGG TGGATCACAC CTGTAATTCT AGCACTTCGG 1560 GAGGCTGAGG CAGGCAGATC ACTTGAGCCC CAGGAGTTTG AGACCAGCCT GGGCAACATG 1620 GCAAAACCCC 1630
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