Tag | Content |
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EnhancerAtlas ID | HS182-11763 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:8438020-8439800 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr2:8438136-8438148 | GGTGACGTCATA | + | 6.02 | CREB1 | MA0018.3 | chr2:8438136-8438148 | GGTGACGTCATA | - | 6.02 | JDP2(var.2) | MA0656.1 | chr2:8438136-8438148 | GGTGACGTCATA | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I008299 | chr2 | 8438730 | 8438931 | GH02I008298 | chr2 | 8439017 | 8439275 |
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Enhancer Sequence | GTATGTGCAC TGTCCTGGAG GACAGTGGCC CATCCTCATA GGATATCATC TCTAATCTGG 60 GCCCTTAACT ATTTACAGAA GGCTCATCCA CCTCTCTGTC AAGCTGGTAG CTTCTGGGTG 120 ACGTCATATG CGATGGGGAA ACTGGAACCC ATGGTTATGT GCCTACTGCT GAATTTCCAT 180 TGCGATAAAA TGGGTTTCTT GACCTAAAGC ACTGTTAGGT GGAACCCTGT GTTGGTGGAT 240 GGTGATGCTG GCGTAGGCCC TGCAGGCAGG AAAGATAAAC TTATGCCAAG ACTATCTGAT 300 GACCCAGGTC TAGAGGAGTC TCTATCCCCT GCATGGGAGA AAAGGTCCAC AGAGCCAACT 360 TGCTACCAAA TAGTTGATTA GTCTCTTTAA AAGACTAATA TGGGGGCTTG GTGTTGCTAG 420 TCTCTGCTGC CAACAGATTA GACATTCAGC AGCAGCAGCA TGTAGAAGAG CCACGGAGAG 480 TGGGAGCCTG TGCTGATGGG CTCTTGCACA GCCTCATTTC TGCAACTAGG GCATCCATTG 540 TTCCTGCACT GGGTGAGACA ATGACAGGCT CACTAATGTC CATCAGCCAA GTCGCCTATG 600 TGGTTGTTTC TGCCCCTTCC ACAGTGAGTG CTCTTTGCTG GTGATCACCA TGTGATACCC 660 AGATCTTCAC ACCCTGCACT CACCCTGATA GGTCCATCCA CAGGCCCCTG CCCCAGACTT 720 CCTTGTCTCT TGTGTTCCAA TCTTTCTCTT TTTCTAACAT CCTACTGCCC ATGAGCCTTG 780 CCATAAATGT CACAGGGCAC ATATGCTTAC CTCAGGCCAC CTCACTTTCC CTACACAGTG 840 GATGACCAGA GGACCTCCCC AGATGGAAGT GCATCAGAAG ACTTCCCCTC ACTGCTGTCT 900 CCCAGGGCCA TCCCTGAGTG TTGCTGCCTG CAATCCATAT TAAATGCACA TGCGCCAATG 960 AATCAAGCCA TCCTGGCCTG AGAGAAGGCG ATCAGTGTAA GCAGATGGAG AAAGAGCAGA 1020 ACAAGAGTGG TGGATGACCT GAGGGCCAAG CAAACCATTT GTGCAACTTC CTTGTTCTCT 1080 CTGGCCCTGC TCATGTTCAG TCCTAGATAT CCTACTTCCC CTTCTGTTGG GCCCACCCAA 1140 GTGTATAAGC AATTGAGTCT GACAGAAACC AGCCCAGCCA TGTGGTTACT CAACCTCGCA 1200 TGATGAAATG CTTCATCTCT ATCAGGGCTG AGAAGCACAC CAGGAGCCAC TTCTCAAATG 1260 ATGTATTCTT TGGTGCTGAT GGCATGGCCT TTCTCCAGAA TGCCAGGAGT GCAGTGATTA 1320 TCCCAGGGCT TGCCATGAGC TCCACATGAT GTCCCTTCCA TACCTCTGTG ATGTATCATA 1380 CGTGCATGCA GTGCCGTCAA GTTCTGCCAC ACCACACCAT AAATGCCACA GAGTACCATA 1440 CAGTTGTCCA GGTCGTATGG CACAAATGAC AAGGTTACTT TCACCATCAT CACCTGGACC 1500 TACTGAGAAT GCTTTTCTTT CTGGGTCCCA ATCAAAGATG ACAGCCTTCC ACACCACCCA 1560 GAAAATGGGT TCAAAATGTG TTCACGAGGG CCAACTATGC TTCCTCCAGA AGCTAAAGAG 1620 GCACCTCAGC ACTGTGCTAC CTCTTTAATG GGAGGAGGTA TGAAGTGCAA TCTCTCTTTA 1680 CTTTGGAGGG ACTCTCCTGT TAAGTCCCTA AAAACTCCAC CAATGTGGAA GGCCTCTAAG 1740 TCTTCACAGG GCTGACCTCC CAGCCTCGCT ATGCATGTGG 1780
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