| Tag | Content |
|---|
EnhancerAtlas ID | HS037-24157 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr3:13342600-13343910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr3:13343141-13343155 | ATGAGTCATCTTTT | - | 7.58 | | KLF13 | MA0657.1 | chr3:13342849-13342867 | CTGCCACGCCCCTCCTGG | + | 6.18 | | KLF14 | MA0740.1 | chr3:13342850-13342864 | TGCCACGCCCCTCC | + | 6.06 | | NFIA | MA0670.1 | chr3:13343776-13343786 | ACTTGGCACC | - | 6.02 | | SP3 | MA0746.2 | chr3:13342850-13342863 | TGCCACGCCCCTC | + | 6.08 | | SPIB | MA0081.2 | chr3:13343205-13343217 | CACTTCCCCATT | - | 6.18 |
|
| | 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 |
| GH03I013301 | chr3 | 13342582 | 13343812 |
|
Enhancer Sequence | TAATGAGACT GTGAAGCCAG CAGAGCCCAC ATGAAGGGCC TCTGACCCTG CCTGGGGCAG 60
CTCAGTCCTC CCTTGCCTCT GGCTCTCATC TCTGGGTATG CTGTCCTAGA CATCTCTCTA 120
TCCATCTTCC CTAGAGCAGG GTCCCTGTTT GCACATATGG GGAAACTGAG GCCCAGAGAA 180
GACAGGGCAG GCGTGAAGTC ACATCGAGAT TCACTCAGTG GCAGAGCTGG GATCAGCATC 240
CAGACTCCCC TGCCACGCCC CTCCTGGAAG CCGGCAGGCC AACATCCCCA GGGACCCTTC 300
CCCACCCCTC ATGAATATTC CCACGGCTGA CCCAGCCCTC CCGCTTCCAG AAGTCTGCAA 360
GAAAACCCAT TACAGATTCA TGAGGCACCT ACTGCATTTC TAATTAAGAG AACACAGTTA 420
TTCTAATTTT AACATCCCTC TCTACTACCT CCGTCCCCTC CCCTTCCCCT GCATTTATAT 480
AAGGGATGTT TCTGCCTCCT GAGAGTGTGA TGCAGCCCGG ATCTCTCGCC TGTTGCTTGG 540
GATGAGTCAT CTTTTGGAGG GCTCTTTGTA ATGCGGGTGA CGCTTGTTCT GAGGTCCCTG 600
ACAGACACTT CCCCATTAAG CAAAGAACAC CAACCCAGGG GCACTGGACC AGGCTGGAGG 660
TTGGAGGGCT CAGCTCCTGT TGACCAAGAC CCTTAAAATA AAATCCAGCC ACCACCCCAG 720
GCCTTCGGGG CTCTGCCTGG GCTTGCCCTG TAACTGACTC GTCTACCCTA GTATAGGGTT 780
GCCAGATAAA ATACAGGGCG CTTAGTTACA CTGGAATTTC AGATAAACAA CAAATCATTT 840
TTTTTAGTAC AAGTATGTTC CATGCAACTT CAGGACACTT GCACTTGAAA AAAATCAGTC 900
ATTGCTTATC TGAAATTTCA GTTTACCTGG CCATCTGGCA ACCTACTCCG GCCACACTGG 960
CCCTTTGCTG TCCCATAATC CCGATAACTT TCCCACCACA GGGCCTTTTC ATGTGCTGTT 1020
CCTTCAGCCT GGGACCCCTA CCCCCACCCC AACTCCCTGA CACTGAGGTC TCACTTCAGA 1080
TGTCACTGCT GCAGAGCAGT CTTCCCTGAG CACCAGACAG AAGTGGGGGC CGCCACCATC 1140
CTCCCTCCTA TGGCCTTGTC TTATCTTTCT CGTGGCACTT GGCACCGCCT TGGAAACAAT 1200
CTTATTTACT GACTTTTCTG TCTCCCCCAC TAGAACATCA GGTCTGTGAG AGAAGCTGAG 1260
CCCATCCAGC AGAGGGCAGG GTGCAGTCAG TGCCCAACGC ATGTGTGTCC 1310
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