Tag | Content |
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EnhancerAtlas ID | HS104-00558 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:16501700-16503780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr1:16503374-16503391 | TGCTTCCTAGGAAGTGA | + | 6.08 | RREB1 | MA0073.1 | chr1:16502026-16502046 | TGTGAGGGGGTGGGAGGGGG | - | 6.61 | RREB1 | MA0073.1 | chr1:16502036-16502056 | TGGGAGGGGGTGGGATGGGG | - | 7.16 | SOX10 | MA0442.2 | chr1:16502839-16502850 | TTCTTTGTTTT | - | 6.62 | ZNF263 | MA0528.1 | chr1:16503057-16503078 | CATCCTCCTCCATCCTCCTCC | - | 6.3 | ZNF263 | MA0528.1 | chr1:16503060-16503081 | CCTCCTCCATCCTCCTCCTCC | - | 8.07 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16501962-16502745 | Colon_Crypt_1 | SE_23091 | chr1:16502844-16503560 | Colon_Crypt_1 | SE_23751 | chr1:16502050-16502674 | Colon_Crypt_2 | SE_23751 | chr1:16502855-16503434 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_24743 | chr1:16502816-16503501 | Colon_Crypt_3 | SE_26540 | chr1:16496436-16504779 | Esophagus | SE_28102 | chr1:16497879-16504574 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16499336-16504399 | Gastric | SE_34268 | chr1:16497740-16504248 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_36144 | chr1:16502024-16503485 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_40833 | chr1:16501759-16503971 | Left_Ventricle | SE_44998 | chr1:16502053-16503662 | NHLF | SE_46140 | chr1:16501795-16503844 | Osteoblasts | SE_47009 | chr1:16502010-16502676 | Ovary | SE_47009 | chr1:16502860-16503560 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16501964-16502662 | Pancreas | SE_47539 | chr1:16502819-16503601 | Pancreas | SE_48744 | chr1:16501448-16503785 | Right_Atrium | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16501918-16504326 | Small_Intestine | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16501943-16502709 | VACO_503 | SE_57939 | chr1:16501961-16502682 | VACO_9m | SE_57939 | chr1:16502843-16503425 | VACO_9m | SE_64726 | chr1:16502266-16503212 | NHEK | SE_65472 | chr1:16498579-16501949 | Pancreatic_islets | SE_65472 | chr1:16501980-16503977 | Pancreatic_islets |
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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 |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | TGGCCCCATA CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA 60 AACCTGGGTT CAGATCCCAC CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC 120 TCGGAGCCTC AGTTTCATGA TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG 180 CTTGAATGAG ATGATGCACT CAGCACGCGG CAGGCCCTGG GGCCCTGTGT GCTCTACAAT 240 TGCAGCTGCT ATTAGACCAG CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA GGCCAGAACA 300 AATCTTGGGA CTGAGTGTAA AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG 360 GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC 420 CTCCCATCCC ACCCTCCACA GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC 480 CGGGATGTGT CTCTCCAGAG CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG 540 GTGGATGCCA GCCCCCGCTG ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG 600 CTCAGGCAGG CCCTCCTCCT GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT 660 GGTGGCTGGT TGCTCCCAGC CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC 720 AGGGGACCTG GGAGAGGCTT CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC 780 AGACCTGAGC CAGTGTCTGG GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC 840 AGGCGGTGAT GACTTGAGTT TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC 900 TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA 960 ACAAAAAAGA ACTTTGAGTG GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC 1020 TATCTCTCTC CATCTCATCA TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT 1080 TCTCTCTGTC TTCCTCTATT TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT 1140 TCTTTGTTTT CCTATCTCTT GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT 1200 TCAGGAGTCA GGAGAGGTAC CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT 1260 AAAATCCCCA GGCGTGCCAC GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG 1320 GGTGTCTAGC AGCGGAGGCT CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC 1380 CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA 1440 GAAAATAATT CTGCAGCTTG AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT 1500 CTACAGCCAG AGACTGGCGC CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG 1560 TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC 1620 CAAACCCACA GTCACCACAC TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC 1680 CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG GTCACCCAGC ACAAGGGTCC CCCTGGAAAA 1740 TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC AGGACAGACA AGCTTTTGGG CCCCCACCTT 1800 TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC 1860 ATGCCTGTAA TCCTAGCACT TTGGGAGGCC GAGGTGGGCA GATCACAAGG TCAGGAGATA 1920 CAGAAGAGAG ACTGGCCACC CATGCACTGG GCCCAGGTCC TAGCTCGACG TCTGAGTCCT 1980 TGTGTGACTG TGAATATGAC TTTTCCACTG GCTGGCCTCA GTTTCCCCAT CTTTGTAACA 2040 GAAGCCTTGC CTTTGCCGCG GATCCCCTCT CTGCTCTAAT 2080
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