| Tag | Content |
|---|
EnhancerAtlas ID | HS101-35614 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:131806290-131808000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00037 | chr5:131804384-131806816 | Adipose_Nuclei | | SE_10340 | chr5:131806848-131810089 | CD19_Primary | | SE_10915 | chr5:131798063-131818030 | CD20 | | SE_11856 | chr5:131806085-131811485 | CD3 | | SE_14495 | chr5:131805826-131811661 | CD4_Memory_Primary_7pool | | SE_16304 | chr5:131806072-131807743 | CD4_Naive_Primary_8pool | | SE_16304 | chr5:131807811-131811139 | CD4_Naive_Primary_8pool | | SE_16894 | chr5:131806916-131808215 | CD4p_CD225int_CD127p_Tmem | | SE_17370 | chr5:131804876-131811594 | CD4p_CD25-_CD45RAp_Naive | | SE_17764 | chr5:131804786-131818044 | CD4p_CD25-_CD45ROp_Memory | | SE_18258 | chr5:131805804-131811428 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19103 | chr5:131805606-131808422 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19972 | chr5:131797758-131816289 | CD56 | | SE_20775 | chr5:131806027-131808256 | CD8_Memory_7pool | | SE_21523 | chr5:131806659-131808149 | CD8_Naive_7pool | | SE_21960 | chr5:131805342-131806664 | CD8_Naive_8pool | | SE_21960 | chr5:131806740-131810211 | CD8_Naive_8pool | | SE_22284 | chr5:131797996-131818026 | CD8_primiary | | SE_25340 | chr5:131788298-131808279 | DND41 | | SE_27629 | chr5:131804613-131806872 | Fetal_Intestine | | SE_28559 | chr5:131804285-131807800 | Fetal_Intestine_Large | | SE_31393 | chr5:131807532-131808086 | Gastric | | SE_37771 | chr5:131804149-131807109 | HSMMtube | | SE_39368 | chr5:131804343-131808265 | Jurkat | | SE_42103 | chr5:131804676-131807088 | Lung | | SE_50023 | chr5:131804207-131809752 | RPMI-8402 | | SE_50051 | chr5:131804590-131808491 | Sigmoid_Colon | | SE_52336 | chr5:131804500-131808314 | Small_Intestine | | SE_53285 | chr5:131804620-131808185 | Spleen | | SE_61818 | chr5:131790756-131837647 | Toledo | | SE_62219 | chr5:131721125-131837948 | Tonsil | | SE_66244 | chr5:131804343-131808265 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr5 | 131807427 | 131807977 | | chr5 | 131806701 | 131807315 | | chr5 | 131806340 | 131806486 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132452 | chr5 | 131788089 | 131817782 |
|
Enhancer Sequence | TACAGACCTT GTTTTATTCA TCCTTATGTC CCTAACCTGG AATGGGCCCA GGGTGACAGT 60
TATAATAAGT GTTTGTCAAG TGAGCAAGTG TGTGGAGTGT GCATTGTAGA GAGTAAGGTC 120
TCTACAGGAT CCTGCTGGAG AGGCAGCCCA CTGGGCTCAC CACTTCTCCA GAGGAGGGAC 180
TGGTCCCTTG CCAGACAGCC CTGCCAGCTG GAGCAGGCTT CCTCAGGGGT GCCTGGAGCT 240
GTTGACCATG GCTGTTGCCC TCTGGCCCCT CTTGGGAAGA GCAACCTGTC AGGTGTTAAA 300
GACGGTCTTC ATTTCTCTTC TCCAAGTAAA CATGACTAGT TTCCATCTCA CCATCTTCTG 360
GCCCTCAGCA GACTGGTTAT CCAGTCTGGA GAGGCAACAG TAGTATCCAG ATGTGATCCG 420
AACAGACAGA ACGATGGATG CAGACGGAAA ATTCAGGTTT GTGTGCTTCG GCAGTCAGTA 480
TATGCAAGTC GTAATGGGGA CAGTGGCTGG CATGGCCTTT AGCACTGTGG GAAGGATCAG 540
GGTGTCTGCC CATCATTTTT CTCTCTTTGA TAGACACTGT TTACGTAGAC ACTGTTTTGG 600
TGTAAAACCC TACGTTGTAG CTCTTGTCAA CAGTGTTATG TTTCTCCTCA ACTGTCCTGG 660
AAACTCCCTG AGGTGGCTGG CTTGTAGGCA CTCCATACCT GTTAGCTAGT ATTATTTATT 720
TATTGTTTTA TTATTTGAAT GGACAATCAA TTCATGTCAT TTAATGAACA TGGGCTATGT 780
GCCAGAAACC ACCAGGTGCC AGAATACAAC ACTGAACTAC AGTAGGCCTG TCCCTGGGCC 840
CCAGAGCTCC CAGACACACT AGGAAGACTT GTTGATTTAA TGATAAACCT TGATTGAGCT 900
CATGATTAAC ATCTTCACCA CCAGACATCA TTGAGTGCTC TCTGTGTGTT CAACTCAGAA 960
CATACCCTTC CTGCCCTCAG AGGCTGGAAT GTGAGAGTCA TTAAGGGAGA CACCATTGTG 1020
GGAGTGAGAA AATCCTGGAC TTGGAGGGAA CTGACTAGGG ATCACCTCCC AGCTCTGCCA 1080
TGGACCCACT GTGTGACCAT GGGCAAGTTA CTTGACCTCT CTGAGCCTCA GTTATCTTAT 1140
CAGTGAAACT GGGTTAATAA TATATCTCTC AGTGGCACAG GAGGATCACA TAGGGTCACC 1200
ACACTCCACA ACTCCAGGAG ATGCTGTTAA CATTTTAGTC TATGGATCCT CTGGTGGCCT 1260
AAGATTTAAA TGAGAGCACT TTTGCTATGT GACCTGAAGT TAATGTCAAT AAGTTATAGC 1320
TATTGTTATG TACGATGTAA GCAGGGGTCA CTGCAGGCCA GAAGGCTGAC ACAATTTGGC 1380
CAGGCTTTGT TCTTCAAGGA AGGGCAGGGC TCTGAGAAGT GCAGACCGTG ATGCAGGTGA 1440
AGGCCAGGAG GCAGGGACTC CCAGGGCAGG TCTGGAAGGA GCGAGGCTGG TGACGGAAGT 1500
GGTCAGCAAC CTCAAGGCAT GAGTAAGGCG CTTGCCCTTC TCTCCAGGCA CAGAGGAGTC 1560
ACTGGAAGCT GGGCAAAGAG CTGGGATGGA TGAGACCAAG GCGAATACTT TACTTATTAA 1620
GCTGCAAAGG ACCCTAGGGA GCATCTTGTC TTACCAGGCA AACAAAGGCC AGGGAGGGAA 1680
AGTAGTGAGT CTCCAGGGTC ACACAGCAAG 1710
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