| Tag | Content |
|---|
EnhancerAtlas ID | HS095-19597 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:31112810-31114710 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr22:31113855-31113872 | GGGTGGGCGGGAGTTAG | - | 7.29 | | TEAD1 | MA0090.2 | chr22:31114134-31114144 | CACATTCCAT | + | 6.02 | | ZNF263 | MA0528.1 | chr22:31114440-31114461 | GGAGGAGGAGGAGAGATGAGA | + | 7.04 | | ZNF263 | MA0528.1 | chr22:31114437-31114458 | GAAGGAGGAGGAGGAGAGATG | + | 7.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 31114035 | 31114170 | | chr22 | 31112825 | 31114124 | | chr22 | 31112958 | 31113917 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I030716 | chr22 | 31112712 | 31116882 |
|
Enhancer Sequence | AGATATATGA TTAGCAAATA TTTTCTCCTA TTCCATAAGT TTCCTTTTTA CTTTGTTGAT 60
TGTGTCCTTC AAGGAACTTA AGTTGTGTCC TTCGATGGAG TCCCATTTGT CTGTTTTTGC 120
TTTTGTTGCC TGTGCTTTTG GTGTCATATC CAAGAAATCA TTGCCAAATC CAATGTCATG 180
AAACTTTATG CCTATGGTTT TCTCTAGGAG TTGTACAGAT GTTACATTTA GGCATTTAAA 240
TCTATTTTGT TTTAATTTTA CTGTTTTTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 300
GTGTGTGTGT AGAGACAGGG TCTCGCTATG TTGCTCAGGC TGATCTTGAA CTCCTGGCCT 360
CAAGTGATTC TCCTACCTCA GCCTCCCAAG TAGCTGGGAT TATAGGCAAG AGCCACTGCA 420
CCTTGCTGGG TCTTTAATCC ATTTTGAGTT AATTTTTGCA TATGGTGTGA GATAAGGGTC 480
TAACTTCATT CTTTTGCACA AGGACATCCA GTTTTTTCAA CATCATTTGT TGAAGAGACT 540
GTCCTTTCCC CCACTGAGTC ATCTTGGCAT CCTTGCCAAA GATCATTTGA CACAGGGAAA 600
AAATCAAGGC CTTTTGAAAA ACGCCTACAC TAAGGGGAAA TGACACATGT TTTACTGTCC 660
AGCTGCAGCT GTGCCATCCA GGACCAGATG GGAAGTTACA TCCAGGAAAG TGGACCTCTA 720
GAGTCCCTTC TCACATCTCT AGGCTTTGCT CACTAGCTAT AAAGCCCTGT ACTTACAAAA 780
AGAATGATTG CCATAGCCTG TAAGAAAGCA GATGGAAGTC AAAAGCAGAT CCTTAGGTTG 840
ATGACAAAGA TTGCTGGTTG AGACTCTTAT TTTGACACTT AGAGTCTCCT TATTCATCTT 900
CTATTCATCT CAAATATGTG CCAACATGAC TCCCCCTCAG GACTGGCCTC ATCTCTGCCT 960
CTCCAGCATC ATCATCTCCT GCTGATCCCT TGCTCTACTC TGACACCTCA GTGACAATGG 1020
GTTGTGTGTG CATTCTGACA GGCGAGGGTG GGCGGGAGTT AGAATCGAGT CCTCAGCTCA 1080
CCTGTCCTCC TGGATCAAGC AACTTCAAAA CACATTGCCC AGTGGTGATT TAAACTCTGA 1140
GGTTAAAGCA GCAGTGGTTT TCTCTTGCTT GAGGGTCCGC AGATGACCAG GCCAGGTCTC 1200
CTTCAGGCAG TGGCACTTGG GAGTAAGCTA GGAGGTGTGT CTTCCTGTTG TGATGGCAGA 1260
AGTACAGGAG GGTAATCGAG AGTCACAGCA TCCCAGCTTG AGCCTGCACA CCCTCACTCC 1320
ATTCCACATT CCATTGGCTG AATCAAGGCA TGTGGCCCTG TCCAATATCA GTAGGGTGGG 1380
AAGATATCCA TTCCCCATTT TAGAGGATCC TACAAAGTCC AGTGGCAAAA GTTGTGCACT 1440
TAAAATTGTA GTTCAGGGAT GGCAGAAAGA AACAGGAGAA ATGCTTCAGT CTGTCACAGC 1500
CTCTAACCTC CCTTCTAACG ATCACATCCT TTAGCCTCTT TATCTATAGA GTGAGAGGAC 1560
TAGGCTAGGT GATGTCTGGG GTTCTTTCTA TCCTTACCTT TCTGAAAATT TGATGGGAAA 1620
CCATCTGGAA GGAGGAGGAG GAGAGATGAG ATATAAAAGA TGACCTGTAT GCTTGGCACT 1680
GGGCTTGGCA CATCAAAGGA CTCGGGAAAT GTCTGTTGAC TTAATGGCTT GGAGATCTGA 1740
GTCCAGGAGG CCAGGAATCT GGTGACTGAC CTGGTAGGGA AAGAATGGGG GATGCTTTAG 1800
CTGGGCCTCA GGTGTTCACT GGCCTTCCTG CCCCTGGGGC CACAGGCCCT GGGCACTGCT 1860
GTTGGAGTTG CAACTTTACA ACTTCGGAGT TGCAGTGACA 1900
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