Tag | Content |
---|
EnhancerAtlas ID | HS007-00148 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:16501660-16503430 |
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 |
|
| 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 |
|
| 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 |
GH01I016171 | chr1 | 16497941 | 16511884 |
|
Enhancer Sequence | GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC TGGCCCCATA CCCCAGAAGC 60 TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA AACCTGGGTT CAGATCCCAC 120 CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC TCGGAGCCTC AGTTTCATGA 180 TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG CTTGAATGAG ATGATGCACT 240 CAGCACGCGG CAGGCCCTGG GGCCCTGTGT GCTCTACAAT TGCAGCTGCT ATTAGACCAG 300 CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA CTGAGTGTAA 360 AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG 420 CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA 480 GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG 540 CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG 600 ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT 660 GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC 720 CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT 780 CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG 840 GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT 900 TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA 960 ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG 1020 GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA 1080 TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT 1140 TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT 1200 GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC 1260 CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC 1320 GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT 1380 CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC 1440 ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG 1500 AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC 1560 CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG 1620 ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC 1680 TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC 1740 CCCTAAGGTG GTCACCCAGC ACAAGGGTCC 1770
|