Tag | Content |
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EnhancerAtlas ID | HS188-13492 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chrX:119829240-119832060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chrX:119831976-119831987 | ATTGCACAATA | + | 6.62 | NFKB1 | MA0105.4 | chrX:119829316-119829329 | AGGGGATCCCCCC | + | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 119829991 | 119830068 | chrX | 119831185 | 119831377 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI120696 | chrX | 119830185 | 119831621 |
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Enhancer Sequence | TAATCAAGGA AACAACCTGA CCCACAGAGA ACGAATAAAA GCAAGACAAC AGCCTACCTA 60 GGAACAACAT GGAGCCAGGG GATCCCCCCG CCACACAGGG AAGCGGTGAC TGAATGAGTG 120 ACCCGGGGAA ACCAGGCTTC TCCCAGGGGG CTGAGCCGCA ACAGCCCACA CACCCCACTT 180 CCATGGCACC TCACAAGATA AGACCCACTG GCTTGGAATT CCAGCCAACT ACCAGTAGCT 240 GCATCGCACC TCCTTAAGAA GGAGTTCCCA GGGGAAGGGG TGGGCCACCA TCTTTGCTGT 300 ATGGGTGTCT TGGCCATTCC AGCCTTCAGA CTTTGGAGTC TGAGCTGAAG GCTGAAGGGA 360 TCCCCCAGCA CAGCACAGCT CCTCTACCAA AACATGGCCA GACTGCTGCT TTAAGCAGGT 420 GCCTGATCCC GTTCCTCCTC ACTGGATGGG ACCTCCCAAT GGGGCCTCTG CCCACCCCTG 480 CCTGAGCTCT CCGGCTGACA AAGATCTTAA TTCTCCCTAG GATTGAGCTC CCGGAGGGAG 540 GGGCGGGCTG CTTCTTTGCT GTTTGGGTGA CTTAGCCATT CCAGCCTTTG GGCTTCAGAG 600 GGTCTGAAGC GATCAGGGGC TGAAGTGCAC TCCCAGCACA GCACAGCTAC TCTACCAAAA 660 CGTGGCCAGG CTGCTTTTTA AAAGCAGGTT CTGATCCCTT CCTCCTCACG GGGTGGGACC 720 TCCAAACTAG GGCCTCCAGC CACTTCCTAC AGGTGCCTTT GGGCCAGCAA CAGGTTTGCA 780 CCTCCCTGGG ACAAAGTTCC CAGAGGGAGG GACATGCTGC CATCTTTGTC TTTTTGCAGC 840 CTTCACTAGT GACACCTCCA GGTTCTGGAA AATCTGAGGT GACTAAAGAC TGAAGCAGGC 900 CCCAAGCATA CTGCAGCAGC CCTACAGAAA AGTGGCCAGA CTCTTACGAT ACACCCGTTC 960 TCCTATCTCC TCACCGGGCA GGTTCTCCAG GCCTGGGCCT CCAGACACCC TGCCACCAGA 1020 GCTCTTGAGC CAGTACAAAC TCAGCAGCTC CCTGTGCAGA TCCTCCAGGG GCATTTGAAA 1080 GCTTCTCTGC CACTGCCCTT GCCACCCTCA GACTAACAAA GGAACAAAGA CCCTAAGTGC 1140 CTTATCCATA CCTCCAACAA GCTGCAGTTG ACCCAAGGAG AGGTGGCCAG TCTGTGTCCC 1200 ACGGGTCCCA CACACCCACC GTGGCTCATC ACCAGGCAGG GAACCCCTAG CTTGGGTCCA 1260 CAGCACAAAC CCTCCATCTT GGGCTGACTG CACTGAGCAA TTGCTGACCT GCATCTCTCT 1320 GGCATAGAGG CCCCAGGAGT CGAGCAAACG ACCCTGGGCC ACAACCATTA CTAAGATCTC 1380 TTCCTTAGCA GCTCTGAGAT TGCCCCAGAG CTGCAGTGGG CAGCCCAAGA GTGCCAAGTC 1440 ATGAACTATG GCCAGCACTT AAGGGGGAGA GGACCCCACA CTTTCAGGGC ACTGAGAGGG 1500 AACACAGCTG CAACTGAGAG GAAACATAGG GGAGCCACAC AACCGGACAA GAGTCTACCA 1560 ACTGACCAAT AAGCCTAAGT GTCACCTGCT GGATCACACC CCAAAGCTTC AACACGAAAA 1620 ATACTTCACT AACATATCCC CCTCTGAAAC CAGAGACAAG ACATCAGCTT CAAATAAAGA 1680 CTCTACACAA AGCCTTGGCC CAGTGAAAAC ATCCAGAAAA GAAGTCTATT GTCTGTACTG 1740 AATCTATGTT GCAGTTTCAT GTGGTTTCTT ACTGTTTCCT TTTCTTTGAA ATGCCAAAGA 1800 GTTGCACAAA TTGAGAATGT CAGGGTTGGA AGTCCCCATA AATGCTGTCA ACTCCAACAA 1860 TGCATCTGGC TCTTAAGTCT TCTGTACAGT TTCTCTAAGT GGTTGCCCAC ATTGTGGTTA 1920 AACACAGCCA ATGCAATGAA AGCAACCACC TGATAGGCAG CCCATGCCAC CTCTCAGCTG 1980 CTGGAAAGCT GTCTTCCCCC TTTAGCAGCC ATCAAATCAC CACCCCTCCA CAGCTGACAC 2040 CAGGCCCTGC CCATCTACCT TACAGGACAT CTCTTGTAGG GTGTATTGAT CTTCCTCGGC 2100 ATCTGCATGT TGCTACCAAC ATGCAGAGAT GAGAAAGAAC CAATGCAAGA ACTCTAGTAA 2160 CTCAAATGGC CAGAAGGCCA TATGTCCTCC AAACGACCGC ACCTCTTGTT CTCTAACAAG 2220 AGTTCTTAAC CAGGCCGAAC TGGCTAGAAT GACAGAAATA AAATTCAGAA TATGGATAGG 2280 AACAAAGACT ATTTAGATTC AGGAGGATGG CAAAACCCAG TCTAAGGGAA ATAAGAACCA 2340 TAATAGAGTG ATACCGGAGC TGAAGGGTGA AATAGCTGGT TTGAAAAAGA ACCTAGGCTG 2400 GGCATGGTGG CTCGCACCTA TATTCCCAGC ACTTTAAGAA GCCAAAGCAG GTGGATCACA 2460 TGAGGTCCGG AGTTCGAGAC CAGCCTGGCC AACATGGCGA AACCCCGTCT CTACTGAAAA 2520 TACAAAAATT AGCTGGGCAT GATGGCAGAC GCCTGTAATC CCAGCTACTC GGGAGGCTGA 2580 GACAGGAGAA TTGCTTGAAC CCGGGAGGTG GAGATTGCAG CGAGCCAAGA TAATGCCACT 2640 GCACCCCAGC CTGGGCAACA GAGTAAGACT CCGTCAAAAA AAAAAGAAGG AGAAGAACAT 2700 AACGGGTCTG ACAGAGCTGA ATAACACAGT ACAAGAATTG CACAATACAA TCACAAGTAT 2760 TAACAGCAGA ATAAACTAAG CTGAGGAAAG AACCTCAGAA CGTGAAATAA GAGAGTCAGA 2820
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