Tag | Content |
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EnhancerAtlas ID | HS104-01082 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:27487830-27489250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:27487853-27487868 | CGAACTCTTGACCTC | - | 6.24 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09350 | chr1:27487738-27488871 | CD14 | SE_23485 | chr1:27487857-27489118 | Colon_Crypt_1 | SE_24258 | chr1:27487876-27488266 | Colon_Crypt_2 | SE_24258 | chr1:27488306-27489028 | Colon_Crypt_2 | SE_31553 | chr1:27487818-27489086 | Gastric | SE_50517 | chr1:27487684-27489162 | Sigmoid_Colon | SE_52500 | chr1:27487781-27489130 | Small_Intestine | SE_53642 | chr1:27487793-27489132 | Spleen |
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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: 1 | ID | Chromosome | Start | End |
GH01I027161 | chr1 | 27487772 | 27489011 |
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Enhancer Sequence | CACCATGTTG GCCAGGCTGG TCTCGAACTC TTGACCTCAG GTGATCCACC TGCTTCGGCC 60 TCTAAAAGTG CTGGGATTAC AGGCGTGAGC TACCACACCC GGCCAAGTCC TCATTTTTTA 120 ACCATTCCAG GCCCACACTG CTTTTGACTC GGAGAGGCCA GGTCTCTGCA GACCCTTCCC 180 CTGCAGATCC AGGACAGCCT CAGGAAGCCT GGACCCTGGG TGGCATCTCC CCCTGCTTAA 240 GCCATGTCTG CTCCCCAATC CCCTCCTTGA ATCCTTTCAC TAAAAGTGCC TGGAGTTTTA 300 TGGCACAAAA TGCATGGCCC TAGGAAAGAA TCTGCTCAGC CCCTATTAGC TGCGCATTAT 360 GAGCAAGTCA CACCTTGTTT CTGTCTCTCG CTGTGTTCAT GTATATGAAA GCTGGGTGGA 420 GTCACATTAC TTGCTTTGTA AGGTTTATTG TAAGGATGAA AAGGCCACTG TATGTCAAGC 480 ATAGTTCCTG GTACACAGTC AGCACGCAGT GACTGGGTTC ATTTCCTTCT TTTGTTTTTT 540 TTTTTTTTTG AGACAGAGTC TTGCTGTCAC CTAGGCTAGA GTACAATGGT GCAATCATAG 600 CTCACAGCAA CCTCAAACTC CTGGGCTCAA CCGATCCTCC AGCCTCGCCC TCCCGAGCAG 660 CTTGGACTAC AGGTACATGC CACCACACCT GACTAATTTT TAAAAATATT TTTGGTAGGG 720 ATAGGGTCTT ACTATATTGC CCAGGCTGGT CTCAAACCCC TGGTCTTGAT TGATTCTCTT 780 GCCTGGGCCT CCCAAAGTAT TGGGATTACA GGGGTAAGCC ATTGTACTCA GCCGCTCCTT 840 CTTTCATCAT AATGTCACAG CCCAGCAAAG CCTTCTTCCA GTCTCCCCGG CACTCACTTC 900 ACCACTGCCT CCTTCTATTT CTCAAACACT GGCAGACACA CTTCTGCCTC AGGGTCTTTG 960 CACTTGCTAT TCCTTCTGCC TGGAACACTC TTCCCCAGAT ATCCACATGG CTGGTTACCT 1020 GACCTCCTTC AAGCCTTTCT GCGAATCTCG CTTCCTGACA TGGCCTACTA TGTTATAATC 1080 CTATGTAATA GTGACACTTC CCCTGCCTGG CCACCACCAC TACCACCCAG CCCCTTCCCC 1140 TGCTCCTTTT TTCTTCTTTG TATAGCATGT TTCACCTTCT CACATACAGT ATAATTCTCC 1200 TATTTGTTAC TTTTATTCTT TTTTTTTTTT TTTTGAGACA GAGTCTTGCT CTGTCACCCA 1260 GGCTGGAGTG CAATGGCATG ATCTCGGCTC ACTGCAACCT CCACCTGTTG GGTTCAAGCA 1320 ATTCTCCTGC TTCAGCCTCC TGAGTAGCTG GGATTATAGG CGTGCGCCAC CATGCCCAGC 1380 TAATTTTTTT TTTTTTTTTT TTGAGACGGA GTTTTGCTCT 1420
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