| Tag | Content |
|---|
EnhancerAtlas ID | HS138-20042 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr2:43671820-43673420 |
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 | | ZNF740 | MA0753.2 | chr2:43671867-43671880 | GTGGGGGGGGAGG | - | 6.87 |
|
| | 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 | CTATTGTGCA GTGAAAAAGG CATCTGGTGA AACGTGTTGA AAAAAAGGTG GGGGGGGAGG 60
TATCCACACA CACCCATTTC TTATACACAC ATCCCATATC ATTCTCGATC ATCTCAGGAA 120
TAGGGATCAA CAGAGTAATG TACAGAGGTA TAAAAAGAAA AGCTAGCAAA GGCAAGCAAA 180
GCCACCATGT AGGAGTAAGG AACTGCATAG GAAACAGTAG TAAAGGTGTG GGTTGTGTCC 240
AGTTTTTAAA AACAGGACTT ATTCACAGGC CATGGAGCAA ACACCATAAA TCTGGTCACT 300
GGATGAAAAC AAATGCTGAA GGCCAAAGCC TGGGGGTTTT CAGTTAGTAT TTCAATCGGG 360
AAGCCAATAA ACTATTAAAA CGGAGCTATT CCCTAGATTC TGGCCTATAA AACCACCCCA 420
CAAGAGAGAA ATCATCTAAC GGCCTGTGTC TCCTCACCAC AGTGATTGCT GATAAAAACA 480
GCAACCTCAT CTTAAGAAAA ATAATCCCCC CATCCCCCGC AAAGGAAACA AACGTACAAA 540
GAAGACAAAG CATGCACATG CGTTTCAAAG GATATGATCA AATGCAAACT AATAAAATAG 600
AAACAACTAA TAAAAAGAAA TCTCAGTTTG AAATCCCATC AGGAAGCCCA TCTCTGATTC 660
TGCTCTTGGA ATCCTCTCAG ATTCTGTTCT TGGAATCCAA TCCCTACCTC AGACTGGGCT 720
GACACTAGCT TTTCTCCCTA GAGTAGTTAA CAAAACAATG AGTGATCAGA AAAGAGATGT 780
CAGGAGTCCC GTGGTCAGAA TCTCACACTC AGGAAGTCTG TGTATTCATA GCGATGGATC 840
TACCAGGAAG CCCTTTCAGG CAGACCATGT TTGAAGGAAA GCATCCTCCT CGGGGCCTCT 900
GTTTTGAGCA CACTGACTGA TCAGGGCTCC AACCAGTATC CTTGTTTCCC TGCCGATCCT 960
CTGTAGGTAG CCATAGGATT TTTGGACTTT TTTTGTTTTT TGTTTTTTTG AGACAGAGTC 1020
TTGCTCTGTC ACCCAGGCTA AGAGTGCGGT AGCACAGTCA GAGCTCACTG CAGCCTCAAA 1080
CTCCTGGGTT CAAGTGATCC TCTTGCCTCA GCCTCCTAAG TAGCTGAGAC TACAGGCACA 1140
TGTTGTCATG CCTGTCTAAT GACGTGTTGT TTTTCTAATC CTTCCCTTTC AGAAGTTGCT 1200
TTCAAGGTGG AGAATTCCCA AATCACTAAA CTGCCTATTA CAATACTATC CTGAGACAGG 1260
GAAGTGAAAG GTCTTGGTCC TGGAAGAGCC CTGCCACGCC CCCTGTGAAG TCACTGGCCC 1320
AAAGGTGGGC CAGGAAACAC ATTTCCACTC CTTTACACAG TGAGTTGGTG AGTAAATATC 1380
AATCTCTTGA ATTCTTCATG TGTGCAAGGT CCCATTTGGG CAGCTTACAT GGGTATTTTT 1440
TAACTAGGAA TTCTTTTTTA GAAAATGTTC CTAAAAAATC ATTTCTAAAA TCTCACAATC 1500
AATTAACTGT TATAGTTTAA TTCAATAATC ATTTACTAAA CAGTTTCTGA TAGACTTTTT 1560
CCAAAGATGG TCAACAAACT TCTATCGTTC CTTATATGTA 1600
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