| Tag | Content |
|---|
EnhancerAtlas ID | HS020-01399 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr1:44029090-44032220 |
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_03403 | chr1:44031827-44032190 | 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_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 | TTTGCCTGGC ACTCCGGGGG ACATCTGAAG TTGGAATCTT ACAGGCTGAG AAATAGCAAA 60
TCTCAGGAGG CCAGAGCCAG GACAGAAGGA GCCCCAGGAA CCGACTCTCC ATGTTGGGAG 120
GAGGTTCCTG AGAGACTGGA GGGAAACTGG GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA 180
AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC 240
ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC TTTGGTGTTG GGAGACAGCA 300
GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG ACTGGAAGGG CCCGAACCTA 360
GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT GAGGTTGGGG AGCCACTGAA 420
GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG 480
CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG GTTGAGTAGG GCGATGTGGG 540
GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG GGGACGCCGT GCCTGCCAAC 600
AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT TAAGATGCCA AGTTTGATGA 660
AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA AACAGCTGAA AATCGAGACT 720
CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC CCCCTTACTG CCTGGAAGCC 780
TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT GCAGATCTGG CAGCCTTCGA 840
CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA GCTGCTGGAG GTGGCCTTGG 900
CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC CTGCCACCTA CGAGGTTCCT 960
TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG TTTTGGCATA GGTGTGTCTG 1020
GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG TGCACCGCCT CTGGATCTGC 1080
TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT GCCCCTCCAC ATGCACATGT 1140
AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT TTCTGTGGGT TCCTGGCTGT 1200
GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA GGCCAGGCCC AACACTCAAG 1260
CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA GGGGGCCTGT GTCTGTGTGT 1320
GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC TGGGTAAACA TGGGTGAAAA 1380
GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG CAAGGCGTCT CCATCTGTCA 1440
GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC ACCCTCAGGC GTCCAAGGCT 1500
GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC TCAGCAGCCT CCACCCCCAT 1560
CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT CCCACCAGAC TCGCCTTGGT 1620
ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA AGGCAGTTTT CCCCTCCTCC 1680
CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT TCTTGAATCT CCCTCCTCCA 1740
GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC GATCAGCTCC AACACTGCTG 1800
TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG ATTCCCACCA TCGACCCCCG 1860
ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT GGGGCAACCA AACCTCTCCA 1920
CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG 1980
GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT ATCTGCGTGA GCCGGGGAGA 2040
CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT AGAATCCGCA AACGGTGTGG 2100
AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC CCCATGGGCT TCTCCTTCCG 2160
TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG TAGTGCAGAC GCCCCCGGCG 2220
CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC AGGGCACCCG GTTGGGGGTG 2280
GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG GAGGATTCCC TGGAGCTGAG 2340
GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG CGGGGGCGGG AAGGGCGGTG 2400
CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG GCACACGCAG CCCTTCCGCG 2460
GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG GCCTGGAGCG GGGAGGGGCC 2520
CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT 2580
CCCGGGGTTG GAAAATGGGT GGGTGCTTGC GACTGTCCAC GTGTGGGGGA CCCTGGGGTT 2640
CGCTTTGCGG TAGATGCAAA CGCCGCGGCG CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG 2700
CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC 2760
ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC CACCCGGTCT CCTCCCAGCC CCACCTCCGA 2820
TTTAGCTGTG TGACCTTGGG CAGGTGTCCA GATGTCTAGA TCTCTCTCAG CCCCTGGTTG 2880
CCCATGTACC TCATAAGGGT TTGGTAAAGA TTTAAGTCAT TTTGTAAAGC ATTTTAACAT 2940
AGTACCTGGA ACCTAGTAAA TGCTTCATAA ATCTTACTGT CCCTCATACC TGGGTCTCAG 3000
TTTTCCCAGT TGTTGATGGG TTTGGAGTGA TCATGTGACA TCATCTGAGG AGTTGCCCAG 3060
GTCCTCAGCC TGAGTGTTGA GGCTGCGGTA GACCCAGCTT CCGCGGGTGC CCGTGGGGGA 3120
AGGTGGTAAG 3130
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