| Tag | Content |
|---|
EnhancerAtlas ID | HS080-18519 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:43671910-43673250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr2:43673110-43673128 | CTGCCACGCCCCCTGTGA | + | 6.05 | | KLF14 | MA0740.1 | chr2:43673111-43673125 | TGCCACGCCCCCTG | + | 6.47 | | KLF16 | MA0741.1 | chr2:43673112-43673123 | GCCACGCCCCC | + | 6.62 | | SP3 | MA0746.2 | chr2:43673111-43673124 | TGCCACGCCCCCT | + | 6.62 | | SP8 | MA0747.1 | chr2:43673112-43673124 | GCCACGCCCCCT | + | 6.92 |
|
| | 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 |
| GH02I043444 | chr2 | 43671764 | 43673179 |
|
Enhancer Sequence | ATCCCATATC ATTCTCGATC ATCTCAGGAA TAGGGATCAA CAGAGTAATG TACAGAGGTA 60
TAAAAAGAAA AGCTAGCAAA GGCAAGCAAA GCCACCATGT AGGAGTAAGG AACTGCATAG 120
GAAACAGTAG TAAAGGTGTG GGTTGTGTCC AGTTTTTAAA AACAGGACTT ATTCACAGGC 180
CATGGAGCAA ACACCATAAA TCTGGTCACT GGATGAAAAC AAATGCTGAA GGCCAAAGCC 240
TGGGGGTTTT CAGTTAGTAT TTCAATCGGG AAGCCAATAA ACTATTAAAA CGGAGCTATT 300
CCCTAGATTC TGGCCTATAA AACCACCCCA CAAGAGAGAA ATCATCTAAC GGCCTGTGTC 360
TCCTCACCAC AGTGATTGCT GATAAAAACA GCAACCTCAT CTTAAGAAAA ATAATCCCCC 420
CATCCCCCGC AAAGGAAACA AACGTACAAA GAAGACAAAG CATGCACATG CGTTTCAAAG 480
GATATGATCA AATGCAAACT AATAAAATAG AAACAACTAA TAAAAAGAAA TCTCAGTTTG 540
AAATCCCATC AGGAAGCCCA TCTCTGATTC TGCTCTTGGA ATCCTCTCAG ATTCTGTTCT 600
TGGAATCCAA TCCCTACCTC AGACTGGGCT GACACTAGCT TTTCTCCCTA GAGTAGTTAA 660
CAAAACAATG AGTGATCAGA AAAGAGATGT CAGGAGTCCC GTGGTCAGAA TCTCACACTC 720
AGGAAGTCTG TGTATTCATA GCGATGGATC TACCAGGAAG CCCTTTCAGG CAGACCATGT 780
TTGAAGGAAA GCATCCTCCT CGGGGCCTCT GTTTTGAGCA CACTGACTGA TCAGGGCTCC 840
AACCAGTATC CTTGTTTCCC TGCCGATCCT CTGTAGGTAG CCATAGGATT TTTGGACTTT 900
TTTTGTTTTT TGTTTTTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTA AGAGTGCGGT 960
AGCACAGTCA GAGCTCACTG CAGCCTCAAA CTCCTGGGTT CAAGTGATCC TCTTGCCTCA 1020
GCCTCCTAAG TAGCTGAGAC TACAGGCACA TGTTGTCATG CCTGTCTAAT GACGTGTTGT 1080
TTTTCTAATC CTTCCCTTTC AGAAGTTGCT TTCAAGGTGG AGAATTCCCA AATCACTAAA 1140
CTGCCTATTA CAATACTATC CTGAGACAGG GAAGTGAAAG GTCTTGGTCC TGGAAGAGCC 1200
CTGCCACGCC CCCTGTGAAG TCACTGGCCC AAAGGTGGGC CAGGAAACAC ATTTCCACTC 1260
CTTTACACAG TGAGTTGGTG AGTAAATATC AATCTCTTGA ATTCTTCATG TGTGCAAGGT 1320
CCCATTTGGG CAGCTTACAT 1340
|
