| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03887 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:212400940-212403540 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:212401139-212401157 | GGAAAGGAGGCAGGGAGG | + | 6.16 | | EWSR1-FLI1 | MA0149.1 | chr1:212403030-212403048 | CCCTCCTCCCTTCCTCTC | - | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr1:212403274-212403292 | GGAGAGAAGGCAGGAAGC | + | 6.39 | | EWSR1-FLI1 | MA0149.1 | chr1:212403008-212403026 | TCTTCCTTGCTTTCTTTC | - | 6.41 | | EWSR1-FLI1 | MA0149.1 | chr1:212403026-212403044 | TTTTCCCTCCTCCCTTCC | - | 6.4 | | EWSR1-FLI1 | MA0149.1 | chr1:212401131-212401149 | GGATGGAAGGAAAGGAGG | + | 6.51 | | EWSR1-FLI1 | MA0149.1 | chr1:212401135-212401153 | GGAAGGAAAGGAGGCAGG | + | 7.18 | | HNF1A | MA0046.2 | chr1:212402044-212402059 | ATTTAATTATTAATC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:212403021-212403042 | CTTTCTTTTCCCTCCTCCCTT | - | 6.09 | | ZNF263 | MA0528.1 | chr1:212403026-212403047 | TTTTCCCTCCTCCCTTCCTCT | - | 6.13 | | ZNF263 | MA0528.1 | chr1:212401156-212401177 | GAAGAAGGAAGAAAAAGGAGA | + | 6.46 | | ZNF263 | MA0528.1 | chr1:212402664-212402685 | CTTTCCTTACCTTCCTCCTTT | - | 6.57 | | ZNF263 | MA0528.1 | chr1:212403018-212403039 | TTTCTTTCTTTTCCCTCCTCC | - | 6.7 | | ZNF263 | MA0528.1 | chr1:212401350-212401371 | CCCTCTTTCCCATCCTCCTTA | - | 6.88 | | ZNF263 | MA0528.1 | chr1:212403029-212403050 | TCCCTCCTCCCTTCCTCTCCC | - | 6 | | ZNF263 | MA0528.1 | chr1:212401347-212401368 | TTTCCCTCTTTCCCATCCTCC | - | 7.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_00506 | chr1:212397824-212401716 | Adipose_Nuclei | | SE_31662 | chr1:212400859-212401451 | Gastric | | SE_31662 | chr1:212401468-212402631 | Gastric | | SE_31662 | chr1:212402726-212404120 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr1 | 212403042 | 212403200 | | chr1 | 212403200 | 212403432 | | chr1 | 212401476 | 212401801 | | chr1 | 212401929 | 212402431 | | chr1 | 212403027 | 212403223 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I212227 | chr1 | 212400860 | 212401451 | | GH01I212228 | chr1 | 212401481 | 212403276 |
|
Enhancer Sequence | TGCCTCCACT GAGGCACACT GGGCCCCGCC ACATTTATTA GCACAAGCCC TGTGATATGG 60
TTGCATAGCT TGCTTTGCTG AACTTGTTGG TTACTAGCTA CTGCTTAATG ACTGGACATT 120
AGAGACTCTT CTGTTGTTTT TATATTCCCA CCACCTCCAC AGCACCTAAC ACACAGGTGG 180
TCAGTAAAAG TGGATGGAAG GAAAGGAGGC AGGGAGGAAG AAGGAAGAAA AAGGAGAGTG 240
GGAAAGAGGC AGGCACGGGC AGGCCCCCCT GCCTCCATGC CAGGTGGGTA CCTGGAGAGT 300
GACACTGTGC CCTCCTGGGA AGCACCCACA CTCCTTTGAT TGGGGGAAAA CGATTCCATG 360
TGGCATGTGC CTTTTGTCCA AATATGCCTT CTTCCTTCGC ATTCTCCTTT CCCTCTTTCC 420
CATCCTCCTT ACCTGAGCAC TAGTTGGGAT CCCTCAGACC TTCTGCTATC TTTAACTTAG 480
TCTTTCCCTC TCTTCCCATA TACAAGATTA ACATTTGACA TTATTTTAAA AATAATCTGT 540
AATAGATTAT CTTTTCCTAC AATCACACTC ATTTTCCCAA TTCCCTGGGA GATAATTCCC 600
ACAAAATTTG TGGTCAGTAA TTAAATTCCT GACCACAATG AATCATGAGG AATATATACT 660
GTGTTCAGAG GGATGGCGTG GTATCCGTAA GGGAGCATCT GCTGAAGGGA GAGAGAGGAC 720
ACATGGGGGT TAGCCCACAA AGCCAAGGGG AGCTGTCCTC CAAACACAAC CAACAGAGTT 780
TAGCTCAGGC TTCAGGATCA AACTATTGCT TCTATTCTGT GTGGAGAGAA CAATGACTGA 840
ATTGGCTGGA ATAGAACAAA GTTGTTAAAG TGAACTTTCT CCACACCTCA TCTCTAATCC 900
CTAAAATTTT GACTTAAACA AAATTTTGAG TTAAGCAAAT TTGAATTAAA AATTTTGAGC 960
AGATACAGGG AATGAATGCA AGAAGCTCTT GATTATCTTC ATGGTGGACT GGCTCATTTT 1020
CATTCCGGGC TGACCTCGTT GATATGTTCT CTACCACTTC TCCTTGCTGA GAAGTAGTTG 1080
GCGTCTATTC AAAGTACACA GGCCATTTAA TTATTAATCG GAGCAAAACA TTATTAGGGA 1140
AGTTAAACTG TTGAGTAGGT GTGTGTGTGT AAACATGTGG ATACTTTCTT GATTATCTAG 1200
CTGTTTTGTT TTGCCTTTTG CCTTTCTGGG TTCCTGCCCC TCTCCATTTG TGGTGATACC 1260
TGTAAGGTGA TTATGCCACT GAATTCCTAA GAGCTTTTTG GTCCCTCTCT CATTCTCCTT 1320
GGATGTGTGT GGAAATGTTT GTCAGCAGGG GCGGACCGGG GAGGGTTCAT GTACACAAGA 1380
AGTGACTGAC CTTGGCCGCT GAGTGGAGTG TGTATTTGTG ACGAGGAAAG GGTTCAGTGT 1440
TTGTGTTTGG TGATGGTTTT ATGTCCTGCT GTCATTAGAG AGGACTTTAT AGGGGTTTCT 1500
GATGACCTAG GGCTCCAGGA ATCATCATGA TTATTTAGAC AATGATTTTA ATGGGCCCAT 1560
ATAAACTTAT TCTGTTTTTA TACTAGTAAC AGAGAAGAAG ATGTTGGAAG ATTAAATATA 1620
GAGAAGGATG GGCTTTAGCG TCACTGTTCA GGGACATTGG GAATTATTCT ACAGAATTCG 1680
ATCCAGCCTA TTCTCATTAT TTCCTTCTTC TTATGACTTT CATTCTTTCC TTACCTTCCT 1740
CCTTTTCCCT TTCTTCTTCT TCTTTTTTTT TTTTTTGAAA CGGAGTCTCT CTCTGCCGCC 1800
CAGGCTGGAG TGCAGTGGTG CAATCTCAGC TCACTGCAAG CTCTGCCTCC CAGGTTCACG 1860
GCATTCTCCT GCCTCAGCCT CCCAACTGGC TGGGACTACA GGCGCCCGCC ACCATGTCCA 1920
GCTATTTTTT TGTATTTTTA GTAGAGACAG GGTTTCACTG CCTTAGCCAG GATGGTCTCG 1980
ATCTCCTGAC CTTGTGATCC ACCTATCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG 2040
AGCCACTGCG CCCGCCCTCT TCTTTTTTTC TTCCTTGCTT TCTTTCTTTT CCCTCCTCCC 2100
TTCCTCTCCC CACCTTTATT TATTTCTTTC AACATGTACT GCCTGCTTAC TATATATTAG 2160
TCACAGTCTA AATGCTGGAG ATGCAGAGAT GAATAACACA TGGCCCCAGC CCTCCTGGAA 2220
CTCAGTTTAG CGTGGGAGGC AGATGGAGGC ACAGATCATT CCAGTACAGT GGTTAACGAT 2280
AGAGATAAGT ACAGGGTGAG CTCAATGTAG GGGTCCCTAA TCCAGCTTGG CTTGGGAGAG 2340
AAGGCAGGAA GCTTCCTGGA AGAGATGATG GCAGATTGAT TGGGAGTGGC TGAAAAAGGA 2400
GCAGGGCTCA AGGCCTTTAC CTGGCAGGCC AGGTCATTCA CATGGTTTAT GAGCACTGGA 2460
TAAAGGGAAT GGGATGAAGG GCTTTGGGGG TATGGGTCTT CCATGAGATA TGACACCAGA 2520
TTTTGATGTC ACTGCATATG GTTAGGACCA CAGGGGCAGG GCAGAAATGA TGTCTACTAC 2580
TGTGGGACAG TACTAGTGAC 2600
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