| Tag | Content |
|---|
EnhancerAtlas ID | HS022-00514 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr1:44029250-44031900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:44031473-44031484 | GGGCGGGAAGG | + | 6.62 | | RFX1 | MA0509.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | + | 6.63 | | RFX1 | MA0509.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | - | 6.63 | | RFX2 | MA0600.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | + | 6.51 | | RFX2 | MA0600.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | - | 6.75 | | Zfx | MA0146.2 | chr1:44031429-44031443 | GGAGCCGGGGCCTG | + | 6.13 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44028518-44030367 | Adipose_Nuclei | | SE_00616 | chr1:44031018-44034110 | Adipose_Nuclei | | SE_03403 | chr1:44028960-44031281 | Brain_Angular_Gyrus | | SE_04240 | chr1:44028929-44032553 | Brain_Anterior_Caudate | | SE_05040 | chr1:44028789-44032962 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44028621-44033904 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44028796-44032406 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44028848-44033378 | Brain_Inferior_Temporal_Lobe | | SE_08920 | chr1:44030094-44030379 | Brain_Mid_Frontal_Lobe | | SE_23829 | chr1:44030959-44031993 | Colon_Crypt_2 | | SE_24870 | chr1:44029728-44030787 | Colon_Crypt_3 | | SE_24870 | chr1:44031008-44032391 | Colon_Crypt_3 | | SE_26649 | chr1:44028759-44032143 | Esophagus | | SE_27645 | chr1:44028997-44029875 | Fetal_Intestine | | SE_27645 | chr1:44031458-44032280 | Fetal_Intestine | | SE_31538 | chr1:44028779-44031982 | Gastric | | SE_33537 | chr1:44028154-44033824 | H2171 | | SE_41575 | chr1:44029231-44029720 | LNCaP | | SE_41575 | chr1:44029923-44031318 | LNCaP | | SE_65452 | chr1:44028737-44032849 | Pancreatic_islets | | SE_69138 | chr1:44029195-44031995 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043563 | chr1 | 44028826 | 44032589 |
|
Enhancer Sequence | GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG 60
GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC 120
TTTGGTGTTG GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG 180
ACTGGAAGGG CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT 240
GAGGTTGGGG AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG 300
GGTCGGGTGT ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG 360
GTTGAGTAGG GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG 420
GGGACGCCGT GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT 480
TAAGATGCCA AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA 540
AACAGCTGAA AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC 600
CCCCTTACTG CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT 660
GCAGATCTGG CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA 720
GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC 780
CTGCCACCTA CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG 840
TTTTGGCATA GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG 900
TGCACCGCCT CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT 960
GCCCCTCCAC ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT 1020
TTCTGTGGGT TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA 1080
GGCCAGGCCC AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA 1140
GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC 1200
TGGGTAAACA TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG 1260
CAAGGCGTCT CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC 1320
ACCCTCAGGC GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC 1380
TCAGCAGCCT CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT 1440
CCCACCAGAC TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA 1500
AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT 1560
TCTTGAATCT CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC 1620
GATCAGCTCC AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG 1680
ATTCCCACCA TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT 1740
GGGGCAACCA AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC 1800
AGCGCAGTTA GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT 1860
ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT 1920
AGAATCCGCA AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC 1980
CCCATGGGCT TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG 2040
TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC 2100
AGGGCACCCG GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG 2160
GAGGATTCCC TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG 2220
CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG 2280
GCACACGCAG CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG 2340
GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG 2400
ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG GAAAATGGGT GGGTGCTTGC GACTGTCCAC 2460
GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG TAGATGCAAA CGCCGCGGCG CGTGTGCGGG 2520
GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC 2580
CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC CACCCGGTCT 2640
CCTCCCAGCC 2650
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