| Tag | Content |
|---|
EnhancerAtlas ID | HS078-09967 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr2:137062400-137064740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr2:137064550-137064560 | ACTTGGCACC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 137063280 | 137063468 | | chr2 | 137063065 | 137063244 | | chr2 | 137063336 | 137063449 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I136305 | chr2 | 137063032 | 137063708 |
| Enhancer Sequence | CACCTTGGCC TCCCAAAGTG CAGGGATTAC AGGCATGAGC CACCGTGCCC GGCCAATTTC 60
TGTTTTAGTT TTTAATACAG AAAAATACTG ATATATATGT GTAATACAGA AAATACTGAT 120
ATATATGTGT ATATATGGAT ATAAAACTCA CTTTATAAAT GAAAGCTCTT TCGGATCTTC 180
AGAATTTCTA GAAGAGTAAA GAGGTCCTGA GACCAAAAAG CTGGAAAACC ACAGTGATAG 240
AGCTGTCAAT ACTCAGCCTG AATAAGGTCA CAGAGAGCTG TGCCTTTCAG AACAAGAAGA 300
ATCCTTGAAA GATGACCTGG CCTTGTTTAC CAAGGCAGAC TAAGTGTTAT CCCTTTTTAC 360
AGATGGGACA ACTGAGACTC CTATCACAGA CTTTACAGAT GCTATACAGC TATTGAGGGA 420
GGAGTTAGGG AGCAGAGTGG GGGTGAGACA GGACCCAGGT CTTATTCCTT CTGATGCAGA 480
CAGAGCTTCA CTCACTAACC TACGCTGTCA GAGAAATGAG TGGTCCCTAT TAAGAAAACA 540
AAAACAACAA ACAGACAAAC CTATCTCCTT CCTTTTCTGT TTTCCTTTAT TAAATTTATC 600
TTCAGCGATT TTGCTGATGA AGGTTCTGAA AGTGCTGGAA AAACCCTTTA TTCGCTCAGC 660
TTCTTAGCAT TTAAAACTTT GGGCTGAGGT TGGTGCTGTC AATAATGCTG GCGGCAATCC 720
TCTCAAGGCT TGACTTGGGG AGCATCTGCT TCCAAGCCCC CTGGAGTGAC TGTTGGCAAA 780
TCTCAGGCTT TTGCTGGCTG TTCACCAGAG AGCTCAGTTC CCTGCCATGT GGGCCTCTGC 840
ACAGGGCCGC TCACAACATG GCAGGTGGCT CTCCTCAGAG TGAGCAAGTG TGTGTGAGTC 900
AGACTGCACA AGGTGAAAAC CACGATCTTC TCGCAACCTA ACCTCAGTAG ACATAGCCTA 960
TCACTTTTGC TGTATTCAAA TTTTAAATTC ACCAGGTCTA GTGCACACTA AAGGGGAGGA 1020
GACTACACAA GGGCATAAAT ACCAGGAGGT GGGGATCCTT GGGGACCATC TTAACGGCTG 1080
CCTACCACAG CCCCTAAATC CAACATCTGA CCCTCTCACT CCTCCAGTGA ATCCACATCA 1140
TCTCACAGTG CCTTCCAAGT GTAAATAGCT TGTGCCCTCT CTCTACAGGC ACAAGCTAGT 1200
GTAGCGGTTA AGAGCATGGA CTCTGAAGCC TGTCTTCCTG GGTTTGAATC CCTGTTCTAC 1260
CACCTGTTAG CTGTTGGCCT CAGGCAAGTT ATTTAACCTC TCTGTGCCTC AGTTTCCTAC 1320
CCACGAAATG GGGATGATAA TTGTTGCTCT TTGATGGAGG CTGTTGTGAA GATTGACATA 1380
ATACACACCA CAGAGTGCTT AAAACAATGA CTGGCATGGA TTAAGCACCA TATAGATACT 1440
TACAGTCATT ATTACTATGT ACCAGAGGCA TTATATAAAT GGTCTTATTG CTAACAATGT 1500
TCATACAAAG TAGGTATTTT CATACCGTCT GACAGGTGAA AAACTAAGGC TTAGACAGTG 1560
TAAGCATCTT GCCCAAGGTA GCACCACTTG TAAGTAATAT GATGGTTATT CTTTCCTAGG 1620
TTTGCATGTC CCAAAGCTGG CCTTCTTCCA TTCACTACAT CTTTAAGAAA TGCACCATGG 1680
AAAGAAAATG GTCATGTGAG AGTTCAGGGA GAACAAGATA AGGATATATG TAACATACTG 1740
CTGATGTAAT TATGAATTAA AAAGGAGACA CTTCTTGAGC ATTCCTGTAT ATACCAATGA 1800
GAGATTTTCT AGGACTAAAT TTTTACTTAG AAAATAAATG ACTGGTAGCC AGGCAGACTA 1860
CAAAATAACC AGTACTTAGG CTATAATTGT TTACCATGTG ATTTTCCCAT GCTTTTCTAT 1920
GGTATTTACC TTGCAATTAA ATGATCAATA GTTATCCTAT AAGTAATAAG TATACCCATG 1980
AAATTTGTGA CCTGGAAAAT CAACCATTAC AAGAGTGGAA GTGTTAAACC GCCTGGAAAT 2040
GATCAGAGAC ATCAAATCCA CACCACTGGG CAGGTAAGGC TGCTTCCTCC CTTTGACACA 2100
TCCATCTAGG CACTAAATTC AGGGATAGCT GAATAAATTC CCAGGCTGTG ACTTGGCACC 2160
ATCTGCAGGT CTTCCCACGT GGGAGCTGGA GCTGCCTGTG GCAGTGTCTC CTTCCAGGCT 2220
GGGAGGGAGG TGCAGCTCTC TAGGTTCCAT TCCATGAAAT TCCATAATGC ATTTCCAGGG 2280
TGAGTGACTA GGTGTGTCCA GTTGTGTTCC AGTGGCAGGT TGCATTGGCT GCTCTTGTGG 2340
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