| Tag | Content |
|---|
EnhancerAtlas ID | HS059-37657 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr5:118624480-118626630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr5:118624499-118624513 | TCTCTTTGAAGTTT | - | 6.05 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_09224 | chr5:118622122-118629762 | CD14 | | SE_10192 | chr5:118622240-118627165 | CD19_Primary | | SE_11647 | chr5:118601731-118629910 | CD20 | | SE_11852 | chr5:118620381-118626089 | CD3 | | SE_11852 | chr5:118626110-118626849 | CD3 | | SE_14409 | chr5:118621860-118626541 | CD4_Memory_Primary_7pool | | SE_15917 | chr5:118624943-118626629 | CD4_Naive_Primary_7pool | | SE_16877 | chr5:118622257-118626581 | CD4p_CD225int_CD127p_Tmem | | SE_17336 | chr5:118602883-118628254 | CD4p_CD25-_CD45RAp_Naive | | SE_17778 | chr5:118617981-118626902 | CD4p_CD25-_CD45ROp_Memory | | SE_18242 | chr5:118602749-118628149 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19112 | chr5:118620683-118627499 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20232 | chr5:118622127-118626787 | CD56 | | SE_22243 | chr5:118621490-118626444 | CD8_Naive_8pool | | SE_22350 | chr5:118602970-118626914 | CD8_primiary | | SE_25388 | chr5:118617272-118628106 | DND41 | | SE_30942 | chr5:118620264-118627099 | Fetal_Thymus | | SE_39376 | chr5:118622306-118627276 | Jurkat | | SE_49946 | chr5:118622292-118627764 | RPMI-8402 | | SE_50308 | chr5:118624984-118625655 | Sigmoid_Colon | | SE_50308 | chr5:118625781-118626786 | Sigmoid_Colon | | SE_55141 | chr5:118624881-118625598 | Thymus | | SE_55141 | chr5:118625905-118626423 | Thymus | | SE_58310 | chr5:118603634-118704575 | Ly1 | | SE_59637 | chr5:118603673-118697862 | Ly4 | | SE_61019 | chr5:118608552-118705688 | HBL1 | | SE_62209 | chr5:118603018-118707327 | Tonsil | | SE_66260 | chr5:118622306-118627276 | Jurkat |
|
| | 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 |
| GH05I119283 | chr5 | 118619196 | 118627084 |
|
Enhancer Sequence | ATTAGACTAA ATACCAGAAT CTCTTTGAAG TTTGTGGATG TAGTCTCCAA AGAGAGAGAA 60
GGGCATTTAA AATTAAACTG CACAGAATTA TAACAAGCAC TTACTACTCA TTCTTGGAAT 120
GAATCTTGCT TTGGCCCTAG GCTAAATTGT CTAGATTTGT GCTCCTTTTG TTGGCTTAAA 180
GCCACATTCA CTCCTTTTTA CAGTGAGAAC CAACTGCTTC CTAGCACGGT TTTGTAGCTT 240
TCTTTTATGG AGGTTCTTAA TTATTTTGCT ATTTCTTTCA TCATGCAGAG TCATTAATAC 300
AAATGTTGAT TCAAAGTAAA TTTACCTGCT GGGCCAGCTT ACCTGTTAGG AATTAGTGTA 360
TTTTATATCA TGATCACACC TTACTATACT TATTGTATAC AATCAAATCT CCTATAATTT 420
CGCAAAGGGA TACTTATCAG ACTTGTGTTC CCAATAGTGT GTATCTTTGT GTGGTATCTG 480
TGGTTTTATT TGTGAAAGAA CTGCCAAAAG ATTGGTCCAG GTTTGTTTCT GTTTTTATTT 540
ATGACTTAAA GAGAGGCATT CGGTCTTACT AGTCACCCAG AGCAGTTTCA CTGGATCCCA 600
AGAAGACCTA AGAGGACTGT TAGGTTTGTA AGAGAAGGAC TGTGCTAGGC TGTACTTAGC 660
CATAACTTCA AGAGAAGACC TGTATTGGGC TGGAAACCTC TTTTAAAGAT TGGAGAATTC 720
AGAAGAAATC TTGTCAAATA AAAACTTATG AAATGCTATC AGTTTCTGGG GCTGAGGCAG 780
GGTGCCTGGC ACAAGGGGAT TCTACCAGGT TCAAGCTGCT TAGACATGGC TGACTGACAC 840
CAAATCCTGT ACATGGCTGC TGTTTATTAT TGCCAGCCTC TTCCTCCTGT TCCCATCACT 900
AATTCTTGCC TTGCTCCAAT GCCCATTTAC CACCTCTGAC ACTTTGAAGC TGCTCTTGCC 960
CTGGGATAAG TTAGGAAAGC CAGAGTGGGA GAAAAGTCCG AGGTAGAAGT GAGGCGAGAT 1020
CTCTCTATAT TTTTGGCAGT ATTTTCTAAA AGCCAGGGCT GGGATCAGAA TTCAGGCTGC 1080
CAGCTGTTAC TACTTTCACA CTACTAAGTC CTTAAAGTTA AAAATAAATT ACAAAATCAT 1140
TCAAAACCAT TATGAAGTCA GTCCAAGACA CAGCTTCACC AACGATTTCA TTAAGTTTAA 1200
AAATTCTCTC ATCATTCAGT CAACTAATGA TTACTAAATG TCTTACTAAA GCATGCAGAG 1260
TTGAAAAATG TTAAAGAAAG AAATTCTCTG CCCTCTAGGA CTTATTAATC TAGTTGTAAG 1320
AAAAATGTTA GGACAGAAAT AATTGGAATG CAATACAGCA TACATAAGTG AAGTGTAGTA 1380
GTTGTCTGTT GCTGCATAAC AGATTACTAA AACTTAGTAG CTAAAAACAA CAAAAAACAT 1440
TTATGGTTAC ATACACTTTC TGTGGGTCAG GAATTTGAGA GCTACTTAGC TGGTTGGTTC 1500
TGGCTTGAGG TCTCCCATAG GATTGTAGTC GGTGAGCTGG CCAGGTCAAC AGATATCTGA 1560
ACATTCTCTG CGGCTGGAGA ATCCAGTTCT AAGCTGGTTC ACTTATGCAG CTGGCAAGTG 1620
GTAGTCGCTC TAGGCAGGAA ATCTCACTTC CTCAATATGT AAACCTCTTC ACAGGTTTAT 1680
TGGAGTGTCC TCATGACATG GTGGATGACT CTTCTTAGAG TGAGTGATCC AAGGGAACAT 1740
AAGGTGGAAG CCTCAGATGT CTCCTATGAT CAAGCTTTGC TTGATCTCCA TTGCTGTTGG 1800
TGTGTGACTT ATTGGTTACA CAGGTCATAT GGGAGGGGAT TACACAAAAG AATGAATATC 1860
AGGAGGTGGG AATCATTGGG GGCATCTTGG AGACTGGCTG TATGAAGAGG CGAAGATCTG 1920
CATAATAATG GAAAGAAGTG TTGGGATGCC TCAAAGGAAG GAGGCAGAAT GTAAAATTGA 1980
TGGATTTTCA GTAGCTGAGG TTGAGGGAAA GGGTGTTGGC TGAGATAGGG CATCAGGAGC 2040
AAAGCAGGGC GGACAGCAGC TGGTGTCAGT GTGTTCAAGG GACATTAATG GAGCAGTGTG 2100
GCTGGAGTAA AGCCTGGTCA GGTAGGAAGG GGTCAGGGCC TGTAGGGTCT 2150
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