| Tag | Content |
|---|
EnhancerAtlas ID | HS147-04236 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:201990910-201992860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:201991522-201991537 | GAGGTCAGAAGTTCA | + | 6.38 | | TBX21 | MA0690.1 | chr1:201992769-201992779 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:201992769-201992780 | AAGGTGTGAAT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:201992213-201992234 | CGCTCCTCCTCCTCCTCCTTC | - | 8.44 | | ZNF263 | MA0528.1 | chr1:201992216-201992237 | TCCTCCTCCTCCTCCTTCTTC | - | 8.69 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:201990827-201991297 | Colon_Crypt_1 | | SE_23058 | chr1:201991682-201993038 | Colon_Crypt_1 | | SE_23723 | chr1:201990919-201991273 | Colon_Crypt_2 | | SE_23723 | chr1:201991793-201992845 | Colon_Crypt_2 | | SE_24689 | chr1:201990748-201991252 | Colon_Crypt_3 | | SE_24689 | chr1:201991746-201993176 | Colon_Crypt_3 | | SE_25977 | chr1:201991449-201992586 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:201991584-201993071 | Esophagus | | SE_27624 | chr1:201991445-201993333 | Fetal_Intestine | | SE_28545 | chr1:201991443-201993383 | Fetal_Intestine_Large | | SE_31432 | chr1:201991670-201993044 | Gastric | | SE_33417 | chr1:201991427-201994657 | H2171 | | SE_33792 | chr1:201990657-201991281 | HCC1954 | | SE_33792 | chr1:201991430-201993180 | HCC1954 | | SE_34304 | chr1:201991505-201993289 | HCT-116 | | SE_34741 | chr1:201990653-201993194 | HeLa | | SE_41626 | chr1:201991969-201992570 | LNCaP | | SE_43434 | chr1:201990679-201991267 | MCF-7 | | SE_43434 | chr1:201991624-201993665 | MCF-7 | | SE_50066 | chr1:201991627-201993065 | Sigmoid_Colon | | SE_52354 | chr1:201991432-201993050 | Small_Intestine | | SE_56834 | chr1:201991684-201992300 | VACO_400 | | SE_56834 | chr1:201992323-201993032 | VACO_400 | | SE_57376 | chr1:201991848-201992311 | VACO_503 | | SE_57945 | chr1:201991851-201992344 | VACO_9m | | SE_57945 | chr1:201992487-201992749 | VACO_9m | | SE_67013 | chr1:201991427-201994657 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAGAAAAGA AAGGTAACTT GCTCAAAGTC ACAAATCATG TTGAATGGAG CCTGAGCTTC 60
ATGTTGACAG CTGACCGCTT ACTGAGTATC TACTAGGTGC CAGGCAATGT GTCAAGTTAT 120
TGCTTTACAT ACATCATTCA TTCTCTCTGT GTTCATTAAC TGTCTGCTGT GTGCATGGCT 180
CCATGCTGTG TGCAGAAGAC CCAGTAGGGA AGAGGTCACC CAGGGGGAGT AGGAAGCCTA 240
GGCTATGGCC TGGCACGGTG GCTTATACCT GTAATCCCAG CACTTTGGGA GGCTGAGGCG 300
GGTAAATCAC CTGAGGGCAG GAATTTGAGA CCAGCCTGGC CAACATGGCG AAACCCCATC 360
TCTAGTAAAA ATACAAAAAT TAGCCGGGCG TGGTGGCGGG TGCCTGTAAT CCCAGCTACT 420
TTGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGAGAGGA GAAGGTTGCG GTGAGCCGAG 480
ATCACACCAC TGCACTCCAG CCAGGCGACA GAGTGAGATT CCATCTCAAA AAAAAAAAAA 540
AAAAAAAATT CCTGGTGCAG TGGCTCAGGC TTGTAATCCC AGCACTTTGG GAGGCTGAGG 600
CGGATGAATC ATGAGGTCAG AAGTTCAAAA CCAGCCTGGC CAAGATGGTG AAACCGCGTC 660
TCTACTAAAA ATACAAAAAA ATTAGCCGGG TATGGTGGCA GCTGCCTGTA ATACCAGCTA 720
CTCGGAAGGC TGAGGCAGAT AATTGCTTGA ACCTGGGAGG CAGAGGTTGC AGTGAGCTGA 780
GATCATGCCA CTGCACTCCA GACTGGGTGG CAGAGTGAGA CTCCATCTCA AAAAAAAAGA 840
AAAGAAAAGA AAGAAAGCCT AGGCTAGAGC CTAGGAAATT CCAAAGACAT CTATATAAAC 900
CTCTCAACAA GGTAGAGGAT AAGTGCCTCA TTTCACAGAT GAGCAAACTG AGGCTTCAGA 960
GAGGTTAAGA AAAGCTTAAG CTCTCAGAGA TAGTAGTAAG TTTAGGAAAC CGGAGCTTGA 1020
ACCCTGCCTT CTTTCTTCAA TTCCACAGCT GACTCTGCTT TGAGAGGTGC TGAGCAACAC 1080
AAATGTCTCC GCTGTATGGG TGCCTAAAAC CCCACCATTA GATGTGCAGT TTGAGGAATG 1140
CCCTATGGAT ATACAAACAT GCCTGGGGTG GAGGGTGGAT TCAATGAGCA TTGCTTTCCA 1200
GGGACCCTTG GATCCTGCAG GGTGGATGGA AAGTGAGTTT TCAGTTCTTC AGAACCTCAC 1260
AGTGGCCAAC CCTTGGGAGC ATTGCCCTCT CATTCTTATC CTACGCTCCT CCTCCTCCTC 1320
CTTCTTCTGC TACGTGCAGG GCTGGGCTGG GGCACCAGCA GCAGCAATTA GCCCAGCTCA 1380
GCCGCCCGTT ACTGGAACCT GCATGTCAAC TCTGGAGCTG ATCCAAGAAA CCACACCCAG 1440
TGTCCTGCAT GACTCAACCT CACCTGCCCC CTCCACACCT GCCAGCCTCA GTGACCCAGG 1500
CCATAGTGCC CAGGGGAAAG TCCCAGCATC CTTTGGTCAA TCCTCATCTA CTCCATGTGT 1560
TTGTAAGGCC AGCTGGGATT TAGAGTCTTT GTATCACAGG CTTGATTCCG GGCTGATTTC 1620
TAGCCAGGAG AGAATGCTCC AGGCGGAGCA AATGCTGGGG TTTGGAAAAC TAGACTCTCC 1680
ATGGCAAATG CAGACAGATG GACCTCCTCT TCACTATCAT TGCTTGAAAC ACGAACAGCT 1740
TAAGGCCATG GGAGATATTA CTTTTCATAT GTCAAATTGG CAAAGAATTA AAGAATGCCC 1800
CTGATGTCTA GAGCTGGTGA GGATGTGAAG AAACTCAAAC TTGACAAAAA CCACTCGTCA 1860
AGGTGTGAAT TGAGAGACAC TTTTTTTTCG AGATGGAGTC TTGCGCTGTC GCCCACGCTG 1920
GAGTGTAGTG GTGCAATCTC AGCTCACTGC 1950
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