| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00725 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:22611340-22613560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr1:22611827-22611842 | GGGTCAGCCTGTCCT | + | 6.6 | | KLF16 | MA0741.1 | chr1:22613246-22613257 | GGGGGCGTGGT | - | 6.14 | | SP3 | MA0746.2 | chr1:22613245-22613258 | AGGGGGCGTGGTG | - | 6.29 | | SP8 | MA0747.1 | chr1:22613245-22613257 | AGGGGGCGTGGT | - | 6.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 22612055 | 22612538 | | chr1 | 22611972 | 22612241 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I022285 | chr1 | 22611843 | 22612951 |
|
Enhancer Sequence | AGAATAAAAA GAGTCTCCAG GAGAGGTGAC ACTGGGAGGG CAGGAGTTTC TGCCCCTGTG 60
GCGTTGACAG TGATGTGGGA AGACAGGACT CCTCCCTTCC CTCACTCAGC AGTGCTAACA 120
GGGCCCAGGA TGGCCTCACC CTGGGCTGGG CCTGGGATCT GGAAGTGAGA TCGCCTGGGC 180
CCCTTCCCCC AGGAGCTCCT GATTCACTAG GGGAGGCAGG TGTGTGGTGT AAGAAGAGCA 240
CCGCATGGAG GAGGCGGTCT GGAGGAGAGC AGGGGTGCGG TGGGTGCTCC AGGGAGGAGG 300
CTAAGTCTGC ACTCAGCCTT GACAAGAGGC ACTCACTGGG AAAAATGAAG CCACAGGTTC 360
CGGATCGTCA GGGCTGGTGC CTCGCATCCT CCATCCTCAT AACTCCCAGT GTGTGGGTGT 420
CCTGAACTGT GTCCTCCTGA CCACCCCTCA CTCCTGGAGA AGCCTCCACA CCAGCCCTCC 480
TTGGTCAGGG TCAGCCTGTC CTCTCTCCTT GTGCTCCCGC GGAGGTGTAG GAAGATGTCC 540
GTTCCGGATG CTGATGAAGA GGAAGGTAGG TACTTGGGCA GGGAAGGTAG AATATGGAGG 600
TTTGGTGAGG ATCTGAGGTC AGGAGATGGG ATTCAGGGCC TCCTTCAGCT ACAGACTCAC 660
GGTGTGACCT TGGGCAAGTC CCCGCCCTCT CCGGGCCTTG GTTGATCCCT CGGTTTGGAT 720
GGGAGAGTTC ACAGGCCTTG TTCCGGCGCC ATTTCTGTGC ATTTGGAGGT GGGGCTGCAC 780
TGGGGCTCCT GGCTCCTGGC CGCGCCGCCT TGCAGCCTAC AGGTCCTGAG TCATCTTCCA 840
GGCAGCGGGT GACCTCTCCA TACCCCTGTC TCCCCGCAGC CCCGTGACCC TGGGCGGCGC 900
GCAGGGCCAG GCCGTCCCAG GCGGGCTGCA CAGTGGAAAT CACAATATTG ACCCAGCGCG 960
CAGGAAGTGG GGAGGACAGG CCGCCGGGGT TCCCGGCCCG GGGGGAGACA GCTCGCTGAG 1020
TGATGAGCTC GGAGCCAAGC TCTCCCTCCC TCCTGGGTCA CCGCACCGCT GCCCGCCGCC 1080
AGGGCTGTTC CTCTTGGCTC CAGGGCCCCC CTCCCTGGAC CTCCCTCCTA CACATTCCCC 1140
CGGCCCAGGC CCCAGAGGGG AGCTGCTGGT GAGCTCCAGG CCTCAGGGCC TCTCGGGCCC 1200
TGCCTCCCTC TAGCCCAAGT CCCGGTTCCC TTGTGCTTCC AGCATCTGAG GGGCCAAAAC 1260
TGGAACTGCA CCCTCACAGG CCACTGACCT TTGGAATAGT CCTGCCTCCC ATTTAACAGA 1320
TGGGGGAACT GAGGCTTAGA AAGGTACTCA GCCAGTTGTA TCAGAGCCAG GATCCACACT 1380
CAGATCTGTC CAACTCCTGG CCAGTGCTCT GTCTACGCCG TGAGTGAGTT ATCGTCGGTC 1440
GTGATAATAG TGTGAGTAAT AAACTGCTCA GTTAGTGAAG TTTTTGGTCT CACGCAGCCC 1500
TCTTGCCTGC CCTAGGAGCG GTTCTGACTT TACAGACGAG GAAGCTAAGG CTTAGAGGTG 1560
GTGAGATAAC TTTCCCAAGG ACACAGCCCG GGAGCAGCAG GGCTGGGATT TGAACTGTGG 1620
TCCGCCTGAT CTGTCTGTTC TGCCAAGCTG TGGGGCAGGA GGGGCCTGTC CTTGAAGGTC 1680
TACTCAAATG CCACCTCCCC TGGGGGGCCC CAGGACCACC TGTAGATTGT GCTCCCCCAG 1740
AGGGGTTCCT TGGGGACAAT GTAGCCCACA GCCTTGCTCT CCAGTGAGGG GGCCCTCAGT 1800
TGGTGTTGCC TGGGGGTCTG GCCGTGGGGT TTGGAGGCTG GTGGGTCAAC CCTGCTGGTG 1860
GGTTGAGCTG GACCAGGAAG TGCTGCTCAG GGGTGAGCAC CCTCCAGGGG GCGTGGTGAA 1920
GTAGAGGGGA AATACTCCTG GGCTTGGAGC TGGGGACCTG GAGCCCCTCC CTAACCTCCC 1980
AGGGTCTTGG TTTCCTCATT CATAGAAAAG GGCTTGGGGT CCATTTGAAG GCCTACTCCC 2040
CAATACCAGA GACTTAGTAG AGCTTTGGGC TTCTATTTCT TCCAGCTCCC TTCCCACAAG 2100
CTGGGTGTCA TGGGGGAAAG GGTTTACAGA GCTCTCACTG GGCTCTGATT AAGTTTTCTA 2160
CCCAGGGTTT TCACTATAAG GAGTCACCAA TGAAAATCTG CCAATGTGCT TCTTCTAGGG 2220
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