| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04262 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:121151210-121152660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:121152096-121152116 | TTGTTGTTGTTGTTTTGTGG | - | 6.72 |
|
| | 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 |
| GH12I120713 | chr12 | 121151781 | 121151990 |
|
Enhancer Sequence | GACCACTAGA CAGTTTTGAG CCAAAGGTCT TTGAAACTCA AATCTTTGTG TGCCACTGCA 60
TCCTGTTTCT TGGACTCCAG TGTGTCCCAC TTCTGTGACC TCTTCCCGTG GCCTGGTCTG 120
CCAGGCATGG TGGTTTGAAG CTGCGTTCAG AGGCTGATGT TTGTTGGATG TCTATTCTGT 180
GCTGGTCACT GTGTTCCACG TCTTTGTGCA CATCAGTGTA TGTAATCCTC ACACCTCTTT 240
GAGGAATTAC TGTTATCTCT GTTTTACAGC GAAGGATCTG AGGCCTACAA TTCCCAGGCG 300
GCTCTTTCCT AAGGCCCTGT GCTGGTTCAT CTTACCATGT TGCCTCCAGT TGGGAAAGGA 360
ATCCTTGAAA TTAAACTATA ATGAGGAAAA CTCACCTGAG CCTGGTGCCC TCTTGGAGGG 420
TGATAGGGAG GATCCTGGTC CAGACATGAG GCAGTTTGAG CCATCTTCTT GCTCTCTTTT 480
ACATATTGCC TTGGAGTTCC CAGACCTAGT TTGGATTTTA ATCTCAACCA TTTTCTGGAA 540
GAACAGACCC AGGAACTCAA CTACTTGGGG TTCCTTAAAT TAGCCTCCCA TAGCCGCTTC 600
CTGTGCTTGT GATAAAGTGC CAGGCTGATC TGGACCACAG AAGCCTTTGG AGCACCTCAC 660
TGGAGGTTTA GCGCCCCCTG GAGTTAGTCA TTTGTTAGAA CACTGGTACA GATACCCATA 720
GTATCAGTGT GGTTTGTAAA CTTACTTTGC AGTGTTTCTC ATCTGATTTG CTACTTAGAG 780
CCTGCAAATT TGATAAGGCC CCGATTTCAC CCCTACCTGG TGGTATTTAT GCTATCATAA 840
TCTCATACTG ACCAAGGCAC CTAAAGGCTC AAGTTCATGG GTAATTTTGT TGTTGTTGTT 900
TTGTGGGTTT TTTTTTTGTG TTGTTTGTTT TGAGACACAG TCTTGGTCTG TCACCCAGGC 960
TGGCGTGCAG TGGCACAATC TTGGCTCACT GCAACCTCTG CCTCCTGGGT TCAAGAGCTT 1020
CTCCTGCCTC AGCCTCCCAA GTAGCTGAGA TTACAGGTGC CCACCACCAT GCCTAGCTAA 1080
TTTCTGTATT TTTAATAGAG ACGGGATTTC ACCATGTTGG TCAGGCTGGT GTCAGACGCC 1140
TGACCTTTGA TTCGCCTGCC TTGGTCTCCC AAAGTGCTGG GATTACAAGC GTGAGCCACC 1200
GCGCCTGGTT GCTTATGGGT AGTTTTTTAT TGGGATGGTC AGATCAAGAC CAGCTAGCTT 1260
CCTGGGTCTG TGGTGTTCTC ATCTCTAAGC CACATATCAC AGTACCTGGG ACATTGCAAG 1320
GACTCCAGGC CTACTACAGG TATGTGGATT TGGATTAGAC TCAAGAGTTG TCATTTCAAT 1380
ATAAGACGGA ACTGTTTCAA GAAGGTCAGC TGAAGATACT GTAAAGTATC TTGGTTTTCA 1440
GTCTCTCTAG 1450
|
