| Tag | Content |
|---|
EnhancerAtlas ID | HS080-19081 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:85183980-85188230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr2:85185844-85185861 | GGGTACGTCCTGTACCT | - | 6.05 | | EWSR1-FLI1 | MA0149.1 | chr2:85184888-85184906 | GCTTCCTTCCTTCCTCTA | - | 6.04 | | EWSR1-FLI1 | MA0149.1 | chr2:85184880-85184898 | TCATCCCTGCTTCCTTCC | - | 6.06 | | EWSR1-FLI1 | MA0149.1 | chr2:85184884-85184902 | CCCTGCTTCCTTCCTTCC | - | 8.57 | | FOXP2 | MA0593.1 | chr2:85186957-85186968 | ATGTAAACAAA | + | 6.14 | | Foxd3 | MA0041.1 | chr2:85185139-85185151 | GAATGTTTTTTT | + | 6.52 | | JUN(var.2) | MA0489.1 | chr2:85186484-85186498 | ATGACTCATTACCT | - | 6.18 | | NKX2-5 | MA0063.2 | chr2:85184248-85184258 | CTCAAGTGGT | - | 6.02 | | NKX2-5 | MA0063.2 | chr2:85187414-85187424 | CTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr2:85188014-85188029 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr2:85187879-85187894 | TGACCTCCTGACCTC | - | 7.19 | | ZNF263 | MA0528.1 | chr2:85188195-85188216 | CCACCCCCACCTCCCTGCTCC | - | 6.12 | | ZNF263 | MA0528.1 | chr2:85187208-85187229 | CCCTCCTCCCTCCACTCCCCT | - | 6.38 | | Zfx | MA0146.2 | chr2:85184773-85184787 | CCCGCCTCGGCCTC | + | 6.01 | | Zfx | MA0146.2 | chr2:85187902-85187916 | CGCGCCTCGGCCTC | + | 6.03 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_24195 | chr2:85185151-85185630 | Colon_Crypt_2 | | SE_25084 | chr2:85185063-85185733 | Colon_Crypt_3 | | SE_27502 | chr2:85184750-85187659 | Esophagus | | SE_32926 | chr2:85184713-85187023 | H1 | | SE_32926 | chr2:85187157-85187722 | H1 | | SE_34685 | chr2:85184438-85187655 | HeLa | | SE_35873 | chr2:85183583-85187716 | HMEC | | SE_47378 | chr2:85183405-85188185 | Panc1 | | SE_52528 | chr2:85184768-85187231 | Small_Intestine | | SE_64856 | chr2:85184623-85187455 | NHEK |
|
| | 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 |
| GH02I084956 | chr2 | 85183648 | 85188352 |
|
Enhancer Sequence | GGGGAATATA TGACTATCAG GTCTCAGTTC CTGGGAGAAT TCACTCACTC ACTCACTCAC 60
TCACTCACTC ACTCACTCAC TCATTCATTC ATCCATTCAA CAAATGCTAT TTGCAAAGTA 120
CTTGGGATTC AAAGACAAAT AAGATATGAT TGCTGTCCTC GAGTAGCTCA GAATCTACTT 180
TTTTTTTTTT GAGACAGGGT CTTGCTCTGT CATCCAGGCT GTTGTGCGGT GACACAATCA 240
TGGCTCACTG CAGCCTCGAC CTCCTGGGCT CAAGTGGTCC TCCCGCCTTA GCCTACCAAG 300
TAGCTGCGAC TACAGACATG CAGCACCACA CCAGGTTAAT TTTTTTGTAT TTTTTTTTTT 360
GTAGAGATGG GGTTTCGCCA TGTTGCCCAG GCTGGTCTCG AAGTCCTGGC TCAAGTGATC 420
CACCCGCCTT GGCTTCCCAA AGTGCTGGGA TTACAGGCGT GTGTCACCAT GCCTGGCCAA 480
GTCTAGCATT TAAACCTTTA ACTGAATGTA AGGGATGAAG AAAAGGGAAT GTGATTTATT 540
TTTTATTTTT ATTTTTTGAG ACGGAGTCTC GCTCTGTCGC CCAGGCTGGA GTGCAGTGGC 600
GCGATCATGG CTCACTGCGA GCTCCGCCTC CTGGGTTCAT GCCAATCTCC AGGCTCAGCC 660
AGTAGCTGGG ACTACAGGCA CCCACCACCC CGCCCGGCTA ATTTTTTTTT TTTTTTTTTT 720
TTTGTATTTT TAGTAGAGAC GGGGTTTCAG CATGTTAGCC GGGATGGTCT CGATCTCCTG 780
ACCTTGTGAT CCGCCCGCCT CGGCCTCCCA AAGTGTTGGG ATTACAGGCA TGAGCCACCG 840
CGCCCGGCTG GGAATGTGAT TTATTAATAA GATCAATGAA TTAAAACATT GAAGTTGCTC 900
TCATCCCTGC TTCCTTCCTT CCTCTAAGCA TCCAGAGAGC CCTCTGATCC TTTGGGATCA 960
CAGACATGGG ATATTTTTAC TCTCCAGCAT GAACACATAG GTGGATTTAC TGTGAAACTA 1020
CTGAAGCTTA CACTTCAGGG TCCCTGGCTT CCTCAAACAG GGCTTCCAAG CCCTATATCT 1080
AATTTTGCAC TTCTTTCTTA AGAGTTGCCT GTACCAAATA TATAAGCCTC AGGGCCCCAA 1140
ACCTGGATCC AGCCTGAGTG AATGTTTTTT TAGAGCCAGG TCTGATAGAA GCCTGTTTTT 1200
AAGGAATTAC CAGGAACTGA GCATGCTGTT TTTGGCCCTC AGGGGTTTCT CTCAGAACTA 1260
AGAATTTGGG GGCTGTCCTC AGTCACAGGT GCAGCCTGAA GTCTGTTCCC GCCATGTTCA 1320
CTCTCCTCTA TTTACCATCA CCTGCCCCTG CTGCGTCTTC CTTTAAAATA CAGCCCTGGG 1380
CCCTAAGCTT TGTGCTGATT CAAGCTCTTT GGAATTCAAG ACATCCAGGA ATCCGACGCT 1440
CCAAGAATTT TCCCAACGAC CTCTCAGTGG GCCATTCAGG CAGGAAAGGA TACACACATT 1500
CCTAATGGGG CCAGGGGCTG TGACTTAGCC TGTGTGTGGC TGAGAGCCTG CTGAATACAA 1560
GGTGCTGGCA GTTGGCAGGG CTTCCCAGGG TGGGGACTTC TTGCTGAGCT CATCAGCAGG 1620
CCCAGCTCTG TACCCATTTG TCCAGGGAAA AACCAACCCC TAATGGAACT GTTTGTTTTA 1680
TACTCTCTCA TCGAAGTCAT AAATGACTCA CAACTAGAAT GTTATTAACG TGAGAACAGA 1740
GGCCTACCTG GCAGAATAAT TGGTTTTGGT CATTTGCTCA GAGTGCCAGG CAAATCCACA 1800
AAGCATATCA AATTACAGGT TAGAAACCTG ATGAATAAAC AAGAATAATA CTGTGAGTTC 1860
TCAAGGGTAC GTCCTGTACC TGTTTTGCCC ACTGTCATAT CTCCGGCAAG ACACAGTGAA 1920
TACAGCCCCT GACACATTGG AGGTAATCTA TAAAGAGTTA CTAAATGATT AAAGAAAAGG 1980
GATGAGCTGT TCTTAGTGGA AACACCCATT TCTCCTAAGA TGAATTCGCA TTCTTTTGGA 2040
CCAGTTCTTT CTAAATTAAC AGCACTACCC AGTGGTATCA GAGCATCTAT ACCTTTGGAT 2100
ATTACAACAA CTCTATAAAT TCTAATTGCT TCTTCTTTTT TTTTTTTTTT TTTGAGACAA 2160
GAGTTTTGCT TTTTCACCCA GGCTGGAATG AAGTGGCGCG ATCTTGGCTC ACTGCAACCT 2220
CCACCCCACC GGGTTCAGGC GATTCTCCTG CCTCAGTCTC CTGAATAGCT GGGATTATAG 2280
GCGTCCGCCA CCACGCTGGC TAATTTTTGT ATTTTCAGTA GAGACGGTGA AGCCATGTTG 2340
GCTAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCACC CACCTCAGCC TCCCAAAGAG 2400
CTAGGATTAC AGGCGTGAGC CACCGTGCCC AGCTGAGACG CTATAATTTC TAACCTATGG 2460
CTTCCCCTTT TCTGGATTCC ATGCAGTCCA CACACAAGCA TTCTATGACT CATTACCTCC 2520
TGAGCATCCA GCTTCTTAAC TGTTACATTC TAGGGATCTT TTCCACAGTA TGTTTCTAAC 2580
TCCTTGATGG TTTTTGGGGG AGACCTGGGT GACACACTTG GAACAGACCT GCTCCAGGGG 2640
CTTGTTACTT TGTGTGCATC CCGCTCCCTT CACTTTCAGG TGACCTCATT TTCTAATCTT 2700
CCTTAGAGCA ACCAATCCCC CATACACTGT CTCCTTCTTC AGAGAATCTT TCTATGTGGA 2760
TTTGTGCTTT TTAAATTGGC ATATGAGTTT TAGGCACAGT TGGACCAGGA AATGCCTTCC 2820
TGAGGAATTC AGCAGCTTCT AGAGATAAAA TGTGATAGAG CAAATTATGA GTCTGGGAAT 2880
CAGGACATCT GGGTTCCAGT TTTGTACACA TCATTCATTT CACAAATAAG CACCCAAAGC 2940
CCACTATGAT AGCCAACTGC AGGGCTGTGC TACAAGTATG TAAACAAAGA CACCTACTCC 3000
TGCCCAAGGG CAGCCCAGTG GGGGAAGTGA AAGGATTAAA TTGCAATAAT AGAGAATTGT 3060
AAAAGGAATT GGGAGCACTT AGTGAGGTGG TTCTACAACT TTATTGCACC ATCAGGATCC 3120
CCACGGGTGT TCTTTCAAAT GCCAATCTTT GAGCCCCATC CTTCAGAGAT CCTGATCCGG 3180
TTGATCTAGG AATGCTCAGG GACATTGAAT GTTTATTCTG AGCACCTTCC CTCCTCCCTC 3240
CACTCCCCTC CTGGTGATTC CACTGGAAGT GGCCCCAACC CACACTCTTT CCTTCAAGAA 3300
AAGGTTCACA AAGGCAGGGG TCTGGAGCTG ATTTTTTTTT TTTTTTTTTT TCCCAAGAGA 3360
CAAGGTGTTG CTCTGTCACC CAGGCTGGAG AGCAGTGGTG CAATCATAGC TCACTGCAGC 3420
CTCAACCTCC CGGACTCAAG TGGTCCTCCC ATCTCAGCTT CCCAAGTAGG AACTACAGGC 3480
ATGTGCCACC ACGTCCAGCC CTTACAGCAC ATCCAGCTCT TACAGCTGAT TTTTAAAGGA 3540
GGAAGGAGTA CAAACTTATG AGGCACAGAG GCAAAAAATG GCATGATTTT ACCCTACGCT 3600
CTAAGAAAAT GAAGGCCATG AGGCATGAAT ACCACAGCTT CCTGACCTAC CCAAATGGAC 3660
ACCTTTATCT CCACTGGCAA TTTTTCTTTT TTGACAGAGT CTCACTCTGT CTCTCAGGCT 3720
GGAGTGCAGT GGCACGATCT CGGCTCACTG CAACCTCCAC CTCCCGGGTT CAAGCGATTC 3780
TCCTGCCTCA GCCTCCTGAG TAGATGGGAC TACAGGCGCG AGCCACCATG CCCAGCTAAT 3840
TTTTGTATTT TTAGTAGAGA TGGGGTTTCA CCATCTTGGC CAGGCTGGTC TTGAAATCCT 3900
GACCTCCTGA CCTCCTGATC TACGCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGTGC 3960
GAGCCACCGT CACTGGCCAA TTTTTGTATT TTCTTAGTAG AGACAGGGTT TCACCATACT 4020
GGCCAGGCTG GTCTTGAACT CCTGACCTCG TGATACACCT ACCTTGGGCT CTCAAAGTGC 4080
TAGGATTACA GGCATGAGCC ACCGCACCCG GCCCATTGGC AACCTTCCTA TAGCACCAGC 4140
AGAGGAAGAG GCATCCTGCT CCTGGTGGAA GCTAAATTTA TCTGGGCTCC TTCTCCCCTC 4200
CATCTCCCAC CCTCACCACC CCCACCTCCC TGCTCCACAC ACACATACAC 4250
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