| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03430 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:212400920-212403540 |
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 | TGCCAGGTGG AAATGGCTGC TGCCTCCACT GAGGCACACT GGGCCCCGCC ACATTTATTA 60
GCACAAGCCC TGTGATATGG TTGCATAGCT TGCTTTGCTG AACTTGTTGG TTACTAGCTA 120
CTGCTTAATG ACTGGACATT AGAGACTCTT CTGTTGTTTT TATATTCCCA CCACCTCCAC 180
AGCACCTAAC ACACAGGTGG TCAGTAAAAG TGGATGGAAG GAAAGGAGGC AGGGAGGAAG 240
AAGGAAGAAA AAGGAGAGTG GGAAAGAGGC AGGCACGGGC AGGCCCCCCT GCCTCCATGC 300
CAGGTGGGTA CCTGGAGAGT GACACTGTGC CCTCCTGGGA AGCACCCACA CTCCTTTGAT 360
TGGGGGAAAA CGATTCCATG TGGCATGTGC CTTTTGTCCA AATATGCCTT CTTCCTTCGC 420
ATTCTCCTTT CCCTCTTTCC CATCCTCCTT ACCTGAGCAC TAGTTGGGAT CCCTCAGACC 480
TTCTGCTATC TTTAACTTAG TCTTTCCCTC TCTTCCCATA TACAAGATTA ACATTTGACA 540
TTATTTTAAA AATAATCTGT AATAGATTAT CTTTTCCTAC AATCACACTC ATTTTCCCAA 600
TTCCCTGGGA GATAATTCCC ACAAAATTTG TGGTCAGTAA TTAAATTCCT GACCACAATG 660
AATCATGAGG AATATATACT GTGTTCAGAG GGATGGCGTG GTATCCGTAA GGGAGCATCT 720
GCTGAAGGGA GAGAGAGGAC ACATGGGGGT TAGCCCACAA AGCCAAGGGG AGCTGTCCTC 780
CAAACACAAC CAACAGAGTT TAGCTCAGGC TTCAGGATCA AACTATTGCT TCTATTCTGT 840
GTGGAGAGAA CAATGACTGA ATTGGCTGGA ATAGAACAAA GTTGTTAAAG TGAACTTTCT 900
CCACACCTCA TCTCTAATCC CTAAAATTTT GACTTAAACA AAATTTTGAG TTAAGCAAAT 960
TTGAATTAAA AATTTTGAGC AGATACAGGG AATGAATGCA AGAAGCTCTT GATTATCTTC 1020
ATGGTGGACT GGCTCATTTT CATTCCGGGC TGACCTCGTT GATATGTTCT CTACCACTTC 1080
TCCTTGCTGA GAAGTAGTTG GCGTCTATTC AAAGTACACA GGCCATTTAA TTATTAATCG 1140
GAGCAAAACA TTATTAGGGA AGTTAAACTG TTGAGTAGGT GTGTGTGTGT AAACATGTGG 1200
ATACTTTCTT GATTATCTAG CTGTTTTGTT TTGCCTTTTG CCTTTCTGGG TTCCTGCCCC 1260
TCTCCATTTG TGGTGATACC TGTAAGGTGA TTATGCCACT GAATTCCTAA GAGCTTTTTG 1320
GTCCCTCTCT CATTCTCCTT GGATGTGTGT GGAAATGTTT GTCAGCAGGG GCGGACCGGG 1380
GAGGGTTCAT GTACACAAGA AGTGACTGAC CTTGGCCGCT GAGTGGAGTG TGTATTTGTG 1440
ACGAGGAAAG GGTTCAGTGT TTGTGTTTGG TGATGGTTTT ATGTCCTGCT GTCATTAGAG 1500
AGGACTTTAT AGGGGTTTCT GATGACCTAG GGCTCCAGGA ATCATCATGA TTATTTAGAC 1560
AATGATTTTA ATGGGCCCAT ATAAACTTAT TCTGTTTTTA TACTAGTAAC AGAGAAGAAG 1620
ATGTTGGAAG ATTAAATATA GAGAAGGATG GGCTTTAGCG TCACTGTTCA GGGACATTGG 1680
GAATTATTCT ACAGAATTCG ATCCAGCCTA TTCTCATTAT TTCCTTCTTC TTATGACTTT 1740
CATTCTTTCC TTACCTTCCT CCTTTTCCCT TTCTTCTTCT TCTTTTTTTT TTTTTTGAAA 1800
CGGAGTCTCT CTCTGCCGCC CAGGCTGGAG TGCAGTGGTG CAATCTCAGC TCACTGCAAG 1860
CTCTGCCTCC CAGGTTCACG GCATTCTCCT GCCTCAGCCT CCCAACTGGC TGGGACTACA 1920
GGCGCCCGCC ACCATGTCCA GCTATTTTTT TGTATTTTTA GTAGAGACAG GGTTTCACTG 1980
CCTTAGCCAG GATGGTCTCG ATCTCCTGAC CTTGTGATCC ACCTATCTCG GCCTCCCAAA 2040
GTGCTGGGAT TACAGGCGTG AGCCACTGCG CCCGCCCTCT TCTTTTTTTC TTCCTTGCTT 2100
TCTTTCTTTT CCCTCCTCCC TTCCTCTCCC CACCTTTATT TATTTCTTTC AACATGTACT 2160
GCCTGCTTAC TATATATTAG TCACAGTCTA AATGCTGGAG ATGCAGAGAT GAATAACACA 2220
TGGCCCCAGC CCTCCTGGAA CTCAGTTTAG CGTGGGAGGC AGATGGAGGC ACAGATCATT 2280
CCAGTACAGT GGTTAACGAT AGAGATAAGT ACAGGGTGAG CTCAATGTAG GGGTCCCTAA 2340
TCCAGCTTGG CTTGGGAGAG AAGGCAGGAA GCTTCCTGGA AGAGATGATG GCAGATTGAT 2400
TGGGAGTGGC TGAAAAAGGA GCAGGGCTCA AGGCCTTTAC CTGGCAGGCC AGGTCATTCA 2460
CATGGTTTAT GAGCACTGGA TAAAGGGAAT GGGATGAAGG GCTTTGGGGG TATGGGTCTT 2520
CCATGAGATA TGACACCAGA TTTTGATGTC ACTGCATATG GTTAGGACCA CAGGGGCAGG 2580
GCAGAAATGA TGTCTACTAC TGTGGGACAG TACTAGTGAC 2620
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