| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04995 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:121655080-121656310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr12:121655985-121655996 | GAGCCATAAAA | + | 6.14 | | HNF1A | MA0046.2 | chr12:121655149-121655164 | GATTAATGATTGACG | + | 6.01 | | HNF1B | MA0153.2 | chr12:121655150-121655163 | ATTAATGATTGAC | - | 6.34 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28089 | chr12:121650430-121657516 | Fetal_Intestine | | SE_28761 | chr12:121646751-121657501 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121212 | chr12 | 121650657 | 121657371 |
|
Enhancer Sequence | TCAGGTGTGT CTCCCACTGT GTCTTCTGTC TAACACTGAC ACCTTGCTCT TTACTGACTT 60
TGCACACTTG ATTAATGATT GACGTGGCCT GAGTCCTGAC ATCACCAATG CCCAGAATGA 120
TTGTTTTAGT CCAAGAAAAC GGTGCAGCCA GATCTCTTTT CAGCTTAGGA TCTAACAGAG 180
TGTATCCAGG CAGCTGTGGT TCCTCAGCTT GAAAGCATGG CAGGCTGAAA GCCCTGAAAG 240
ATGAGAAAAC AAATGTCTTA AATCCTGATA GAAATTCAAG TGGAAATATC ACCTTTCCAC 300
ATTTTGGGTT TGCATTATTG TCCCAAATAC ACGAGGTAAA TCTTTTCAGA CAGTGTAAAA 360
ACTTTAGGCC GGGCACAGTA GCTCACGTGT GTAATCCCAG CACTTTGGGA GGCTGGGGCG 420
GGCAGATACC TTGAGCCCAG GAGTTTGAGA CCAGCCTGGG CAATGTGGTG AAACCCCATC 480
TCTATAAAAA AAAAAAAAAA GAAAAAAAAA GAAAAGAATT AGAGACCATT AGAGACCAAA 540
ACCCAAACAA GAAGGAAACA GAGACAGCAG CACAGGACTC CATCGGGAGC GAAAGGAAGG 600
GAAGACATTG TTTACTGCTG CATACTAGTC TTCAGGCTGT TAATCTGCAA AGCTCCAAGT 660
TAAACATTGA CTCTTTAGTC CTGGTAACAG CTCTGCACCA CACAGTCAAA CCCGACATAG 720
CCCTCCAGAT GGCCTATGTG CTAAGGGACC GAGGGCGACC AGTAGAGATA AGCTGCCAAC 780
TCTTGGCTCA GAGCTCTTGC CAGGGAAAAC AAGAACTCCA GAAACTCTTT CTTCAGGTGT 840
GTTCTTCCCC CTGCCTTCTC AAGAGAAGGG TCTTGTGGGG TCCCCAGAGA GGAGACCGAG 900
CTAATGAGCC ATAAAAGTCA GGAGGAAGGG CCAGGTGCGG TGGCTCATGC CTGTAATCCC 960
AGCACTTTGG GAGGCCGAGG TCGGTGTATC ATGAGGTCAA GAGATTGAGA CCATCCTGGC 1020
TAACATGGTG AAACCCTGTC TACTAAAAAT ACAAAAATTA GTGGGGTGTG GTGGTGGGTG 1080
CCTGTAGTCC CAGCTACTAG GGAGGCTGAG GCAGGAGAAT CTCTTGAACC TGGGAGGCGG 1140
AGGTTGTAGT GAGCCGAGAT AGTGCCACTG CACTCCAGCC TGGTGACAGA GCAAGACTCC 1200
GTCTCAAAAA AAAAGATCAA GTGGAACAGG 1230
|
