EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS032-00898 
Organism
Homo sapiens 
Tissue/cell
DLD1 
Coordinate
chr7:44672480-44675320 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GLI2MA0734.2chr7:44675092-44675107CTACGTGGGTGGGCT-6.93
HNF4GMA0484.1chr7:44674404-44674419AGGGTCCAGAGTCCA+6.09
Klf1MA0493.1chr7:44674996-44675007TGGGTGTGGCT-6.14
NFIAMA0670.1chr7:44673611-44673621ACTTGGCACC-6.02
POU4F2MA0683.1chr7:44673340-44673356TTGCATAATTATTGAG+6.32
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_09293chr7:44668114-44680616CD14
SE_12002chr7:44669441-44675480CD3
SE_14587chr7:44668357-44680825CD4_Memory_Primary_7pool
SE_15490chr7:44672497-44675949CD4_Memory_Primary_8pool
SE_16434chr7:44672525-44680593CD4_Naive_Primary_8pool
SE_16951chr7:44669426-44675446CD4p_CD225int_CD127p_Tmem
SE_17851chr7:44668129-44680829CD4p_CD25-_CD45ROp_Memory
SE_18656chr7:44670100-44680815CD4p_CD25-_Il17-_PMAstim_Th
SE_19294chr7:44669461-44675423CD4p_CD25-_Il17p_PMAstim_Th17
SE_20655chr7:44668188-44680617CD56
SE_21218chr7:44672481-44680578CD8_Memory_7pool
SE_22840chr7:44672479-44680608CD8_primiary
SE_24636chr7:44672874-44674105Colon_Crypt_2
SE_24636chr7:44674149-44675329Colon_Crypt_2
SE_26120chr7:44672338-44680827Duodenum_Smooth_Muscle
SE_27427chr7:44672693-44675348Esophagus
SE_27654chr7:44668239-44680825Fetal_Intestine
SE_28557chr7:44668586-44680821Fetal_Intestine_Large
SE_32407chr7:44672719-44680093Gastric
SE_34691chr7:44670606-44681894HeLa
SE_36719chr7:44672712-44674454HMEC
SE_37328chr7:44672508-44680850HSMMtube
SE_40682chr7:44672552-44680631Left_Ventricle
SE_42075chr7:44672899-44675402LNCaP
SE_42544chr7:44672671-44680682Lung
SE_43768chr7:44668130-44675212MM1S
SE_46384chr7:44672195-44675458Osteoblasts
SE_48519chr7:44672671-44680588Psoas_Muscle
SE_49693chr7:44672888-44674157Right_Ventricle
SE_49693chr7:44674163-44674856Right_Ventricle
SE_49693chr7:44674881-44675350Right_Ventricle
SE_50531chr7:44672686-44677149Sigmoid_Colon
SE_52560chr7:44672691-44680563Small_Intestine
SE_53907chr7:44672618-44680662Spleen
SE_62947chr7:44653723-44680812Tonsil
SE_64825chr7:44672758-44674454NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr74467494144675231
chr74467284644675300
Number: 1             
IDChromosomeStartEnd
GH07I044628chr74466800844681598
Enhancer Sequence
ATTATCCTTT TGTACTGTAC TTTAAGAAAA AAAAAATTTT GTTTAATGTC AGAAATTGAA 60
AGGGGAGAGA GATCAAAAAT ACCTTAATGG GGCCAGGCAC AGTGGCTCAC GCCTGTAATC 120
CCAGCACTTT GGGAGGCTGA GGTGGGCAGA TCACGAGGTC AGGAGATCGA GACCATCCTG 180
GCTAACATGG TGAAACCCTG TCTGTACTAA AAATACAAAA AATTAGCCGG GCATGGTGGC 240
GCACCCCTGT AGTCCCAGCT ACTTGGGAAG CTGAGGCAGG AGAATGGCGT GAACCTGGGA 300
GGCGGAGCTT TTAGTGAGCC AAGATTGAGC CACTGCACTC TAGCCTGGGC AACAGAGCGA 360
GACTCTGTGT CAAAAAAAAA AAAAAAAAAA AAACCCTCAA TGGGAAAGTA GACTCCAAGA 420
GTGAAAAGGA GCAAATTGTT CCAGTGAGTT CCATTCTGTA GCACAGGTGG CCACAGGTGC 480
TTGCCTTTGA GGAAATGAAA GAGCCATGCT TTGTAAGTCA GAGGCAGGCT CAGCTTCCCC 540
GCACAGTCTG AAGCTGGGTG GCGGTGAGAA ATTACTAAAA GGTTAGTGCC GGTTTTTTAG 600
ATGAAGTCAT CATGTTATTA AAAAATAGTC TGTTTAGTCT CTAGGTTACT GTTCTCTGGC 660
TCCCCTCCCC ATCCAAGACT CCCTTGGAGG GAGGTTTGAG GACTTTGGGA TTCTCATATC 720
TCTTCGCGTC CATGATTGGA TCGTGAGGTG AGGAGATAGC CTTTAGAACC CTCTCTTTGA 780
GTGGTCAGTC ACGTGGTATT CCCTCTGAAA CCCTGGAGCA GATGCTTTGT GTAGCTGGGC 840
TGGGGTTCCC CCAAATAGGG TTGCATAATT ATTGAGGACA GATGAGGCCT CAACCAGACG 900
ACCACAGGTG ACCCCAGACT GTGGGTCTTC CTCACCTCCT TGAGAGTTGC AATTCTGAGA 960
GCTGATAAAA TGTGCCATTG TGTGCAGATC TGGGTAGTTT GAAGCGTTCT CATTTCCTGA 1020
GGTGTGTCAG AAAGACTGCG TGAGAAAGGG GTCACAGTAT CTTGGATGTC ATCTTTTCAT 1080
GCAGTAAAAA GTCTGGTTTC CATGAATGTT TGTATAACAA ACCACCTCAA AACTTGGCAC 1140
CAGTGTAGCA TGTCTCATGA CTCTGTGGGT TGGCTAGGTT TCCCCACTCC TCCCACTGCC 1200
AGCTCCCTTG GAGCTGAGGC TCACACCAGG CTAGAAGCCA TGAAGGCCTC TGATGTGTCT 1260
GGCAGTTTGT GCTGGCTGTT CACTGGGCCC TGCCATCCTC CAGTAGGCCG GAGCGATTCC 1320
TGCACAAAGT CCCAGAGTAG CTCCAGACAG GGAAAAGAAA GGCTGTGGGG CCTTTGAGGC 1380
CTAGGTCCAG ACCGTACACT GCTACTCCCC ACGCCATTAC CTTGGTTAGA GCAAGTCACA 1440
GACAACCCTT AGGGACATCC GTTTGGGGAG AGGAAAAGGC ATGGCCACTG GACAGCCCTC 1500
CACAGCTCTT TTCATAATGA CCTGATAGAG CAGCCACCTT TAGTCTAGTG CAGAATCCCA 1560
GCAAATATCA TTCTGATATC AGTAGATTCC ATAGGGCAGA GCTGAAGCAG CTGTTCTTTG 1620
CTAATCTTGG AAGTTTATTG ATGTTTTATT TACACACCTG TACAGACAGA AGATAATAGA 1680
GATTGTTTAG AAATATTCTG TCACCTATAA TGACTAAGCA TTGCTATAAT GGAGCATGTG 1740
GTTTCCTTAA TTGAAGAATA CCTAAATAGA AGCCCATTCT TAACTGGCCT CAGTATAAAC 1800
AGCTTGTAGT GGCAGGTCAC CAGGCCTGGA TCACAGTGCC CTACCTTGTT TTTGCTTCAT 1860
AGGCAGAATG GTGGTAAGTG GTACTCTGGC CTGGGCAAGG TCTGAGCAAG GCCTGCATTG 1920
ATGGAGGGTC CAGAGTCCAG CTCTACCATC TGCACATTTT CTTTGGAGAC TTGTGCTTAG 1980
CCCAACAGCA TGAATCATTT GCTGAAGGCT CTGGAGGTGG GCATTCCATC CACAAGTCTC 2040
CCCAATAGGG AGTACCCTGT TTGGACATAC AGGGTAGTCA CACATATGGG TTTTAAATCT 2100
TGTTCTTAGG ATATTTTCAG GAAAAGCTCT GGCCCACACG TTTAGGACCA TTTCCTGGGC 2160
AGCATTGGAA GGAGTGGTAG AGGTCATGCA GGCCTGCCCT GTCTTGTGTG CAGGAAAAGA 2220
ATGAGTTGTT GGTCTACACT GAGGCCGGGA TGGGAGGCCT GCCCCTTACA GCAGCGCCGG 2280
CTGAACTCCA GGCTGGCTGG TCACATGGTG CCCAGCAGCT GACTTTTTAT CAGCTTGGCT 2340
GGATTAGAAT GAGCTGAAAG AAGAGCCATA CGCCGGTGTT CCTTGGTTAC ATGGTGCCCT 2400
GTAGTTGATA TTTATAGCAA TTAAAAAGCA TTGTCAGTGT CAGAACTTAG TAAGTGAGGT 2460
TGTGTGGATA GTGCTGGGCC TCATCAACTT ATCAGCTGTG CGAGGGCCTT TGAGCATGGG 2520
TGTGGCTCCA TGCAGCAAGG AGACCGGAGC CTGCCCCACC CGCGCCGCGG ATTATTTAGA 2580
CAAGGTGGCA GTAATGTGGT GACCAAGGGT AGCTACGTGG GTGGGCTGGG CTTGTTCTGT 2640
GGCTGAGGTG GAGTAGGGAG GGCAGCTGGA GTGGCGTCTG TAGGGGCTAT GGATAGATGA 2700
GAGGAAGTGG TCTCATCAGT CCAGAGCCAC CCGTAGTCAT AGAGCTTGGG CTAAGTTGTA 2760
ACACTCTCCT CATGTTCCTC ATCAACTTCT TGAACAAATG CAAGTATATG TGCAAGGACT 2820
TTATAATTTT TTTTTTTTTT 2840