EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS159-05632 
Organism
Homo sapiens 
Tissue/cell
Pancreatic_islet 
Coordinate
chr7:44677940-44680600 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr5a2MA0505.1chr7:44679698-44679713GCTGACCTTGACCCT-6.88
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_09293chr7:44668114-44680616CD14
SE_12002chr7:44675737-44680602CD3
SE_14587chr7:44668357-44680825CD4_Memory_Primary_7pool
SE_15490chr7:44676270-44680378CD4_Memory_Primary_8pool
SE_16434chr7:44672525-44680593CD4_Naive_Primary_8pool
SE_16951chr7:44675465-44680529CD4p_CD225int_CD127p_Tmem
SE_17851chr7:44668129-44680829CD4p_CD25-_CD45ROp_Memory
SE_18656chr7:44670100-44680815CD4p_CD25-_Il17-_PMAstim_Th
SE_19294chr7:44675433-44680659CD4p_CD25-_Il17p_PMAstim_Th17
SE_20655chr7:44668188-44680617CD56
SE_21218chr7:44672481-44680578CD8_Memory_7pool
SE_22840chr7:44672479-44680608CD8_primiary
SE_24636chr7:44677846-44680063Colon_Crypt_2
SE_26120chr7:44672338-44680827Duodenum_Smooth_Muscle
SE_27427chr7:44675393-44680685Esophagus
SE_27654chr7:44668239-44680825Fetal_Intestine
SE_28557chr7:44668586-44680821Fetal_Intestine_Large
SE_32407chr7:44672719-44680093Gastric
SE_32407chr7:44680106-44680586Gastric
SE_34691chr7:44670606-44681894HeLa
SE_36719chr7:44676722-44680551HMEC
SE_37328chr7:44672508-44680850HSMMtube
SE_40682chr7:44672552-44680631Left_Ventricle
SE_42075chr7:44679237-44679954LNCaP
SE_42544chr7:44672671-44680682Lung
SE_43768chr7:44675436-44680621MM1S
SE_46384chr7:44676438-44680713Osteoblasts
SE_48519chr7:44672671-44680588Psoas_Muscle
SE_49693chr7:44677999-44679961Right_Ventricle
SE_50531chr7:44677170-44680609Sigmoid_Colon
SE_52560chr7:44672691-44680563Small_Intestine
SE_53907chr7:44672618-44680662Spleen
SE_62947chr7:44653723-44680812Tonsil
SE_64825chr7:44676532-44680626NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr74467939244679514
chr74468010144680272
chr74467862244679047
Number: 1             
IDChromosomeStartEnd
GH07I044628chr74466800844681598
Enhancer Sequence
CTTACTTCAT AAAGAAACCA AAGTCTGACT GCCTCCATTT CTCATGAGTG AAAAACTGTT 60
TCTATTATAG GAAACTTAGG TCTTCAGTGT GTTTGATGGT AGCATGCTAT TAGATTGTGT 120
ATTCTCAAGT CTGATTTTCC CCATTACTGT GCTTTCTCCT TTTCACTTCT GCTTTGTCAC 180
TTGGAATGTT TCTAGAAGTA GAAGTCACTG CCCCTGCCTA CATCAGACTG CAATTCCGGG 240
ACATCCAGGC AACAGCAAGG GATAATTAGG AATAAATTTG GCTGGAAGAA AGGGAAAATG 300
CAGCTTAGGC AGCCTAAACC AACAGGCTTA TTTTTCTCAC TCAGTAAGAG AGCTGAGGTC 360
GCCTGACTCA GCTCAGGTTC TCAGTGAGCC ATCAGCCACC AGGTGCCACC TTTCAGTGAG 420
TGGGCTTCTA TCCCTTCCAG GTGTCTCTTC ATGCTCCATG GGAATTAGAT GGGACATGCT 480
TTGACTCTCT CTTCCAGAAG CTTTCTCTTC TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT 540
GGTCAATGAC TCAGCCTAGT CTTGATTTAT CCCCCAGGAT GGGGACAGAC AGCAGGGGAG 600
AGATCTCAGG TTGAGATGAG TGTACAGTAA GGGCTGGGAG TATCAGAAGG GGAAACGCTC 660
TCCCAGATAG TGACAAAGCT AAGCGACCAT GTGAAGGGAG AGGACAAACA TCCCATGGAA 720
AGAAGGGTAG CTGCCAGGCC TGCGGGAAGG AAGGAGCATG ATGCTGGGGC ATGGGAGCAA 780
GTGGACAGGG AGGGCTCTGC AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG 840
ATCCAGATTC AGGTGTTCAG AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG 900
AGGTATCTCC TTGGGGAGTG GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA 960
GGTGGAAAGA GAGTGGGGGA TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC 1020
CCATTGGTGA CTCATACAGG GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT 1080
GGGCAGGTCT GGCTTCCTGC TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA 1140
TGACCTTCAT TTTCAAAGCC TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA 1200
TATTAAAATT CACTTGTTTT AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC 1260
ACTACACTCG ATACAAAACA TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG 1320
GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC 1380
AGAATGGGCT CTTTGTCTGA AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG 1440
CCAACTGGAG AGTGAAGTGG GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG 1500
TTGCATTCCC AGCATTTTCC TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA 1560
CCAGTTTTTT TCTGACTGCC TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA 1620
GCCAATTGAA AATCACCTGG AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG 1680
CCCGATGATC ATGATCGCCC TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT 1740
GTGGCTCAGG ACCAGAGAGC TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC 1800
TGGAAATTCC TTTCATTTTA TTGTTGAGCC CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT 1860
AAGCTAGGGT AAGAGGCACT GTTACTAGAG TGACCAGAGT TCTTTAAGCG TCGCTCTGCT 1920
ATTACTCAGT TAACCTTATT AATACCCTGC CTGGTGACTG CTGTGTGTAA ATTCTGCCTG 1980
AGCCCACATC TCTCCAGTGG GAATATGATT GACATTCCAG GTGCTCTAAG TAAGTTGGAA 2040
AAGCCCACAG AGAGCCTCAG TAAAAGTTAG CTATACCTAT CCCTGCTGCT ATTGGTGGGT 2100
TTTTTTTGTT TTGTTTTGTT TTACTATTTT AATTGTTATT CAAAGCTAAT TTTATTGAAA 2160
AGAAGTAAAC TTGTGATTTT GCTATGACTT TTGGCTCTGG ATCCAAAAGT GAATATTGTC 2220
CCCTAGGATA AAGGAGGCTG TCTGTACAGC TGGAGAGACT CTTGATCTAA GGTCTTGCTC 2280
TTGGGTGACT TTGCCCTGTG TTTCTGGACA CTTAATGGGT TTTACGAAAT AGAAGAAAAT 2340
GTTTTAGGGG TTTAATAAAG TTTGGGTTGT GCTGTTCTCC AGTACTTACT GGGTTTGAGG 2400
GTCATGCCCT ATCCATGAAC CTGTTGTGGC CCCAGGGAAC TAAGTAAGTG TCTACAGCTA 2460
GACTTGGGGT GCGGGTCACA TGGTGTGAGG GTAGACATTC TAGCACTGGA GCAAGTTTGG 2520
GGTAAAGAAA AATTTTGATT AGGTTTTTTG TGGGTTTTTT TTTTTTTCTT TGAGACAGAG 2580
TCTCGCTCTG TCGCCAAACT GGAGTGCAAT GGCATGATCT CAGCTCACTG CAACCTCCGA 2640
CTCCCTGGTT CAAGTGATTG 2660