| Tag | Content |
|---|
EnhancerAtlas ID | HS113-01969 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:111734980-111737190 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr1:111735350-111735367 | TGCTTTTAAGGAATTCA | + | 6.75 | | MSC | MA0665.1 | chr1:111737042-111737052 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:111737042-111737052 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:111737042-111737052 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:111737042-111737052 | AACAGCTGTT | - | 6.02 | | RELA | MA0107.1 | chr1:111735541-111735551 | GGAAATTCCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
| SE_00548 | chr1:111731103-111739856 | Adipose_Nuclei | | SE_09820 | chr1:111732766-111737633 | CD14 | | SE_10666 | chr1:111734737-111736772 | CD19_Primary | | SE_11520 | chr1:111707642-111752738 | CD20 | | SE_11981 | chr1:111734412-111740334 | CD3 | | SE_14851 | chr1:111732908-111748239 | CD4_Memory_Primary_7pool | | SE_15648 | chr1:111735190-111736704 | CD4_Memory_Primary_8pool | | SE_15989 | chr1:111735276-111736505 | CD4_Naive_Primary_7pool | | SE_15989 | chr1:111736681-111744339 | CD4_Naive_Primary_7pool | | SE_16482 | chr1:111734952-111737246 | CD4_Naive_Primary_8pool | | SE_17180 | chr1:111734752-111737483 | CD4p_CD225int_CD127p_Tmem | | SE_17406 | chr1:111727560-111749237 | CD4p_CD25-_CD45RAp_Naive | | SE_17935 | chr1:111728556-111748584 | CD4p_CD25-_CD45ROp_Memory | | SE_18363 | chr1:111727276-111748673 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19522 | chr1:111734154-111744848 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20205 | chr1:111734731-111748565 | CD56 | | SE_21249 | chr1:111734884-111744812 | CD8_Memory_7pool | | SE_21711 | chr1:111735057-111739495 | CD8_Naive_7pool | | SE_22036 | chr1:111733937-111748137 | CD8_Naive_8pool | | SE_22415 | chr1:111732656-111748767 | CD8_primiary | | SE_24170 | chr1:111735373-111736163 | Colon_Crypt_2 | | SE_24170 | chr1:111736828-111737638 | Colon_Crypt_2 | | SE_25351 | chr1:111732691-111754239 | DND41 | | SE_27328 | chr1:111734461-111737751 | Esophagus | | SE_30932 | chr1:111734917-111736739 | Fetal_Thymus | | SE_32304 | chr1:111734292-111735250 | Gastric | | SE_32304 | chr1:111735305-111736259 | Gastric | | SE_32304 | chr1:111736753-111737709 | Gastric | | SE_32464 | chr1:111734374-111749255 | GM12878 | | SE_50246 | chr1:111732689-111748417 | Sigmoid_Colon | | SE_52868 | chr1:111732755-111744865 | Small_Intestine | | SE_53613 | chr1:111731924-111739395 | Spleen | | SE_55120 | chr1:111735211-111735666 | Thymus | | SE_58401 | chr1:111735195-111775083 | Ly1 | | SE_62234 | chr1:111732684-111775273 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 111736343 | 111736397 | | chr1 | 111735402 | 111735659 | | chr1 | 111735691 | 111736003 |
|
Enhancer Sequence | ACCACCATGC TACACACCCC TCATCGCCCA CCACCAACAG CAGCTAGAGC AGTGCTGCCC 60
ATGCCCATGG GCAGAAAGGC AAGTCTGGGG GCCATGCTGG TCACAGAGCT TGAACGTACA 120
TTGCTGGGAG GGAGGGACAG AAACTAGAGA GTCTGAGGCT TCACTATCAA GAAGGGCCTT 180
GATTTGACCC TTCTTTTCCC AGTTAGTCTT CTCAACTTAC TACTGGCCAA AAATAAAAGT 240
GACTCTGAAG AGAAGAGGGA AGAAGAGTTG CTTTCATTCA AGGAGATAAT TGATTGAGCC 300
CCTAGCCTGT GCTCACAACT GTGAGCATAC CTCACAGATG TGGATACCAG GAAGAGTAAG 360
ACACTGACCC TGCTTTTAAG GAATTCACAG TGTAGTTAAG AGACAAACAT GTAAACAAGC 420
ACTGGAGGCT CAGCCGAGAG GCAAAGCCTT TTTACCTCGC TATGTCTATC CACCCTCATC 480
CCCAGCCTTT GCCCCCACAC AGCCCCCTCT GGGCACACTC GAGGTTATTA AAGATTACCA 540
GGTTGCTGCC TGAGTAGCTT GGGAAATTCC CAGGTTCTAG GAACCTCTGC CCAGCAATTC 600
CTACACGGAA AGTCCCACAA AGGTGCCTCC TCAAGACTTT CCAGTGAAGC ATTTCTCGTC 660
ACTCCTGCCC AAGTCACAAC TTGGACCCTA CTCCTCTCGC CACCACATAC ACACAGTCCC 720
ACTCTCTGTC TTTCTCTTTT ATCCCCTGGC TTTCATGGCT CTTCTTTACT CCAGCCAAAT 780
TGCCTCAAAG TCAAGGCCAA TAAAAGCACA GATGCGGGAA TCCTTGTTTC AGTTCTGGGT 840
TTCAAGCTGG CACTTCCTGA ATTAGCAAAA TTGAGTCTCT GAGAGGCTAG CTGACTGGAA 900
GTCCCCTCCC TGTCCGAGCT TCAGGGAGCT GAAAAACTCA GTGTGGGAAG GAAGTGGGGA 960
GTGGTGGGAT TTCCCTGAAG AAAGTAAACG TCTGAGAGGT GAATCCTGCC GACCTCCACT 1020
TCCCAAACAC TGATCTGAGG AGGAAAGGCA GAATCCCAGC TCTAGCCACA CAGGAATTTC 1080
TGGTTTCCAT TCAAGGCTGG GAGTGAAAGA GCTATTTCCA AAGCAAAAGA TGATGCCACT 1140
CCCTTCAAGG ATTACCTACA ACTAGTTCCT CTTTGGTTAT CACCCATTTT TACAGAATCT 1200
TCAACACAGA GACCCCACTG CTTGCCCAAG TTTCCTTTCC TCTGAAACCC ATGGCATTCA 1260
CCTGCCCCTC TGACTTCTGT TGAGTCCCTA ACATCCTTTT CTTCTTCCCT AAAAGATAAA 1320
AGCAGGGTTG TCAACCTAAA ATCACTGGTT TTCTCCCTCC CCAGATATGA ATAGAAGGTC 1380
TACCCCTACC CCTACTGTTT TATGACTTCT TTCATTCTCC ATTCTATTAC ATCTCCCCAC 1440
GTCCTTCTCA GATCTGAAGC CCCTAAAAGG TAGAGACCAT GGCACAATAG TACCCTGCTT 1500
CCACTATACA CAGGGATATA CTCAACTGTG AACTTAAGAA CAGAAGCTAG CACTCAGCAA 1560
TATGTGCTCA GCAGGGTGTT AGGTACCTAA TGTGCATTAT TTCATTTAAT CCTCACCACA 1620
ACCTTATGAG GTAATCACAA TCATTATTTC CATTTTTAAG AAGTTAACAA ACTAACTTAA 1680
TGGGAACCTC ATAGCTAAAG GTAGAAGAAC TGGATTTAAA CCTCCTAATT CTGCTGATTT 1740
CAATCCCTGT GCTTTCAACC AGTATGTAAT TCCGCATCCC CTTCAGGTGA AGGACCTTGT 1800
CCTGTTTGTA TCTTCCCAAT GCTTGGCATC TGGCAACCAG TTGACACACA ATAAATGTTT 1860
GTTGAATGAG TATCTACCTC CTGCCCTGTT CTCCACCCTC CCTCAGCCTT GCAAGGGCAG 1920
AATCATGTCT GCATCCACCC TAACTGGTCC CACCCAGGCT GTCCCAGGAA TACTTCCTGT 1980
CCTTCCCCAA GCTAAGTCAG GAGCATTCCT CAGGCCCAGG CAGCAGTCCT GTGTGGAGGA 2040
AGAGGCAGTG GGGGTGGTTC AAAACAGCTG TTTCTCTTGG TTTAAAGAAC AAGGAGCTAG 2100
AAACAGGAGG GTGGGCGCAT GGACCCTACA GCCCATTTTC CTTGGATAAC CTCCAGTCTG 2160
TTCCCTTGAA CCCAGGGATG CTGGGCAGTT CAGGTGAGCC GTCCAGGGGC 2210
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