| Tag | Content |
|---|
EnhancerAtlas ID | HS136-10018 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr2:8437480-8439800 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I008299 | chr2 | 8438730 | 8438931 | | GH02I008298 | chr2 | 8439017 | 8439275 |
|
Enhancer Sequence | CCCCCATCCT CAATTCGCAC CTCTGCTGGT CTACGTAGCT TGCCTAGTGA GGCAGTCCAG 60
ACCATCATCT CTGAAGGGTC TGCACCTCTA GTTATCATTC CCTTTGCAAG CTATGACATC 120
TGCACTTGGC CACTTGTAGT TAAAACTGAG CATGGGAGCA CCAAGAGACA CCCCGGTGCA 180
TCCTCTGAGC AACAATCAAT TCTGCCCTGG CCCTGTGCAT CCTCAGCCCC ACTTCCCCTG 240
GCCAGCTGTG CCCACCAGGA TGATATCTCC CTTCCTTTAT GGCTGATCCT TGTCATGAAG 300
ACTCTAAGTG ACAAAGTGGC TGGTGTAAAT TAAAGTTCGT TGGGACTTTT GCTGTGTCCT 360
CCTGCAGAGG CATCCTTGCT CTGCAAGCCA GGATCTCTAC ACCCACAGAA CCTCATATGT 420
CAGAGAAAGA AAGCACACAT TCCCTAAGTA GGTCACTGGG GGTGTTGCTA AGTACGGCTG 480
CTCCTACTAC TATTCTTTTC TTTGGTTCCA ACCTATTTGG GACACAGCAG CATTGACATA 540
GTATGTGCAC TGTCCTGGAG GACAGTGGCC CATCCTCATA GGATATCATC TCTAATCTGG 600
GCCCTTAACT ATTTACAGAA GGCTCATCCA CCTCTCTGTC AAGCTGGTAG CTTCTGGGTG 660
ACGTCATATG CGATGGGGAA ACTGGAACCC ATGGTTATGT GCCTACTGCT GAATTTCCAT 720
TGCGATAAAA TGGGTTTCTT GACCTAAAGC ACTGTTAGGT GGAACCCTGT GTTGGTGGAT 780
GGTGATGCTG GCGTAGGCCC TGCAGGCAGG AAAGATAAAC TTATGCCAAG ACTATCTGAT 840
GACCCAGGTC TAGAGGAGTC TCTATCCCCT GCATGGGAGA AAAGGTCCAC AGAGCCAACT 900
TGCTACCAAA TAGTTGATTA GTCTCTTTAA AAGACTAATA TGGGGGCTTG GTGTTGCTAG 960
TCTCTGCTGC CAACAGATTA GACATTCAGC AGCAGCAGCA TGTAGAAGAG CCACGGAGAG 1020
TGGGAGCCTG TGCTGATGGG CTCTTGCACA GCCTCATTTC TGCAACTAGG GCATCCATTG 1080
TTCCTGCACT GGGTGAGACA ATGACAGGCT CACTAATGTC CATCAGCCAA GTCGCCTATG 1140
TGGTTGTTTC TGCCCCTTCC ACAGTGAGTG CTCTTTGCTG GTGATCACCA TGTGATACCC 1200
AGATCTTCAC ACCCTGCACT CACCCTGATA GGTCCATCCA CAGGCCCCTG CCCCAGACTT 1260
CCTTGTCTCT TGTGTTCCAA TCTTTCTCTT TTTCTAACAT CCTACTGCCC ATGAGCCTTG 1320
CCATAAATGT CACAGGGCAC ATATGCTTAC CTCAGGCCAC CTCACTTTCC CTACACAGTG 1380
GATGACCAGA GGACCTCCCC AGATGGAAGT GCATCAGAAG ACTTCCCCTC ACTGCTGTCT 1440
CCCAGGGCCA TCCCTGAGTG TTGCTGCCTG CAATCCATAT TAAATGCACA TGCGCCAATG 1500
AATCAAGCCA TCCTGGCCTG AGAGAAGGCG ATCAGTGTAA GCAGATGGAG AAAGAGCAGA 1560
ACAAGAGTGG TGGATGACCT GAGGGCCAAG CAAACCATTT GTGCAACTTC CTTGTTCTCT 1620
CTGGCCCTGC TCATGTTCAG TCCTAGATAT CCTACTTCCC CTTCTGTTGG GCCCACCCAA 1680
GTGTATAAGC AATTGAGTCT GACAGAAACC AGCCCAGCCA TGTGGTTACT CAACCTCGCA 1740
TGATGAAATG CTTCATCTCT ATCAGGGCTG AGAAGCACAC CAGGAGCCAC TTCTCAAATG 1800
ATGTATTCTT TGGTGCTGAT GGCATGGCCT TTCTCCAGAA TGCCAGGAGT GCAGTGATTA 1860
TCCCAGGGCT TGCCATGAGC TCCACATGAT GTCCCTTCCA TACCTCTGTG ATGTATCATA 1920
CGTGCATGCA GTGCCGTCAA GTTCTGCCAC ACCACACCAT AAATGCCACA GAGTACCATA 1980
CAGTTGTCCA GGTCGTATGG CACAAATGAC AAGGTTACTT TCACCATCAT CACCTGGACC 2040
TACTGAGAAT GCTTTTCTTT CTGGGTCCCA ATCAAAGATG ACAGCCTTCC ACACCACCCA 2100
GAAAATGGGT TCAAAATGTG TTCACGAGGG CCAACTATGC TTCCTCCAGA AGCTAAAGAG 2160
GCACCTCAGC ACTGTGCTAC CTCTTTAATG GGAGGAGGTA TGAAGTGCAA TCTCTCTTTA 2220
CTTTGGAGGG ACTCTCCTGT TAAGTCCCTA AAAACTCCAC CAATGTGGAA GGCCTCTAAG 2280
TCTTCACAGG GCTGACCTCC CAGCCTCGCT ATGCATGTGG 2320
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