EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-55333 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr3:46988670-46991290 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr3:46989860-46989871AGAGATAAGGA-6.02
NR2F1MA0017.2chr3:46989541-46989554CAGAGGTCATGGG+6.22
RARA(var.2)MA0730.1chr3:46990879-46990896AGGTCACACAGAGGGCA+6.61
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00943chr3:46987333-46991985Adrenal_Gland
SE_02008chr3:46987772-46990525Aorta
SE_11155chr3:46963907-46992913CD20
SE_13638chr3:46988105-46991652CD34_Primary_RO01536
SE_14564chr3:46984749-46992585CD4_Memory_Primary_7pool
SE_16650chr3:46987830-46991302CD4_Naive_Primary_8pool
SE_18708chr3:46986099-46991562CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46985017-46993140CD56
SE_22640chr3:46985615-46991406CD8_primiary
SE_23114chr3:46987260-46991352Colon_Crypt_1
SE_23749chr3:46987346-46991294Colon_Crypt_2
SE_26114chr3:46983078-46991394Duodenum_Smooth_Muscle
SE_27142chr3:46983018-46992857Esophagus
SE_28145chr3:46982939-46992085Fetal_Intestine
SE_28630chr3:46982992-46992260Fetal_Intestine_Large
SE_30558chr3:46988988-46991255Fetal_Muscle
SE_31407chr3:46987243-46992180Gastric
SE_32585chr3:46989343-46991413GM12878
SE_38780chr3:46987824-46991550HUVEC
SE_40617chr3:46975387-46993135Left_Ventricle
SE_41619chr3:46988621-46991305LNCaP
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46987822-46991381Pancreas
SE_48306chr3:46987919-46991489Psoas_Muscle
SE_48684chr3:46987782-46991986Right_Atrium
SE_49453chr3:46987803-46989682Right_Ventricle
SE_49453chr3:46989698-46991296Right_Ventricle
SE_50160chr3:46987309-46992159Sigmoid_Colon
SE_52388chr3:46987277-46992190Small_Intestine
SE_53507chr3:46987802-46992203Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_64772chr3:46987179-46991025NHEK
SE_65471chr3:46977753-46993036Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr34698953346989702
chr34699043746991167
chr34698877546989017
chr34698868646990431
chr34698973646990203
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
AAGAAGAGGC CAAACTGGCC CCACTTTGAG CCTTTCCAGT TCTGATTTGG GCCCAGGGTG 60
GGGAAAAAAG CAAAAGAGAT GGGCACATAG TGCCTGAAGG TGACAGGAAG AGACAGACAA 120
TGCTGGGGCA AACTTGGCAG GCTCCCCAGT GTCACCTTGT GCCCATCCTC AGGGCCACTG 180
CAGCCCCATG CCGGGGTGGA GGGACTTCCT GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT 240
CCAAGGGCAC TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG ACTCACCCTG AAGATGGAGT 300
GATAAGAAGT GAGCTGAACA CCACCATGCC TGGGACCAGA AACTGCACAG ATCTCTACTG 360
CCCAGAGACT GGCAGGGGGA AAGGGGGAGA GACTCTGCTT CTCCTGGGCA GGCTGAGATC 420
TCGTCAGGCT GCAGAGCTCC TCACTCTGGG TCCCCTGCAC TCAATGTGCT GCTAGGATGA 480
CTTGGTCCGA GTATCCACTC TATCTGCTGA CCAGACCAAG AGTTCCTAGA GGGCAGACGT 540
TTGTTGTACC AGTTTGCACC CACAGGCCTG ACACCAACTA CAGCAGGCAC AGCACTGTGG 600
TAGAGGAGTG CACAGGAGCG GGGAAATCCC AGCTCCATTT CATCTTGGCT GTGTGACCTT 660
GGGCAAGTTA TATGACCTGT CTGGCCTCAG TTTCCTCATC TACAAAAATG AGGATAATCA 720
TACTGACATC ATATCACCAT TACAAGGAAA TGATGAAGGA GAAAAGCCTG CAGCTTAGGG 780
AGCCTGAAGA ACAGGGAGAA TCAGGCCAGG GCAGGAAGGA AAGGGCTGCA GAAAAGCCAG 840
CGGGGCACAG GCCCAGAACG GTGTGCCTCT GCAGAGGTCA TGGGAAGCTC CCATGCCCAT 900
CATCCTTATC AGATGTTCTC AGCAATCCTG TAAGCAGACA GGGCAGTGTT GTAATACCTG 960
CTTCACCAAG ACATTAGGAG ATGACGTCAG ATGATCTGTG CAGTGTAGAC AGATCTGATT 1020
CCCCATTCAG TGCTTCACCA AGAGTCAGCA GGAACAGGTG GTGACTACCA TCCAAGAGGC 1080
TGGGATTAGC TAAGAGCCAC TGCTCTCCTG TGGGTTCATG TGTTCCCTAA AGGCTTCTGA 1140
GCAGAGCAAG AACAAAGCGC TGAGCGGGAG GCTGGGAGAA CAGCGAGGCT AGAGATAAGG 1200
ACTGGAGATA AGGACGGGAA CTAGGTCAAC AGCGGTGGAC TAGAACAAGG AGGTGCCTCA 1260
ACGCTGTGGG GAGACAGGGA GGAGCAGAAA CAACTGAGGT TCTGCTGGTG ACTCACTGGG 1320
GGAAGGAAGG CGCCTTTGAC AAAAAGGTGG TGGCACTTAG GGGACAAAGA GAAAGGGTGT 1380
GGCAGCCTTC AGGCATTCTA ACGGTGAGGC TTGACACCCA AGGCCTGACG AAGGTTGGTG 1440
CCAAGGGATA GCACCTGTCA AGGTGCCCTC AGCGGTGGAA AGGAGGGCCC GCTCCACTCA 1500
GAAGAGAGGC ACGCTGGGCC CCACCATCCA TATGGCACCT CAAGGGCCAG GCCACGGCAT 1560
GCCTAGTGCA GCTCCTCGCC AGGCCCGTCA CACGGCCCTG CCCAGATATC CTCCATGTGT 1620
CTGTCAGGAG TGTGGGGAGC CAGCCCAAGT CAACTCTGAT CCTATTCTTG CTGCAAGTGC 1680
TCAAGGGAGG CACTACAGAG CTCCTCCAGC AGACTTTATC AGTCGACAAA TACTGACTGG 1740
CTCCCCTGTG GTACTCCATG CTGTACTCAG ATACTCCATG CTGGGTACTG AGGAGGAAGA 1800
GGAACGAGTA GGCACCTAGT GCCCACAGAG CAGGGCAGGG GTTCTTATCC TCGGTGCACA 1860
GATTCCAGAG GTCAATGACC AGACAGAAAC ACAGGCGAGT GTGAGAAGGT GAATCTTAGT 1920
GGATGAGAAA TCTGGAGCTC TTCAGATTCT CAAGGGGGTG GTGACCCACA GGGGAAAAGG 1980
GAAGGTGTCA ACAGCCAGGG AAGGCAGTGT TTTTTTGGGT GGCATTAAGA GGTGTCTACA 2040
GAGGCTTTCC AAAGGAAGTG TCACCTTAAA GGATGAGTGA CAGTGGGGAC AGAGGGACGG 2100
AGGGGGAAGA GAGCAGAGGG AACAACCAGA ACCATTAGTA TGCAAAAGGC CCCTCCCACT 2160
GCCCTGAGAC TTCACCCACA CTGGCCCCAG CAGGAAATAA CCTCTTGAAA GGTCACACAG 2220
AGGGCAGGGC AAAGACCAGT CTCTTCCCCT TCCTTCATAT GCAGCCAGAC TGGACGAGTT 2280
CCTCTGGGAA GTCTGGCCTG GCTCCAAACT CCCTCCAGGG TCCTCCCTGT AGGGGCACTG 2340
TGGTATGCAG GAAGCCCAGC CTGCAGCCCT GGACTGGGCA GGTGGTGGGA ACATCAGGAC 2400
ACACTGCTTA CCAGTGGTGG GACCTCCCTG AGGCTCTGTC TCCTCCCCTG TCAAAGTGGG 2460
GCTGGCACTA CTTTAACAGG GGCATGTGAG GATTATACAA GGCAACTTGG GTCCACCATG 2520
TGGTACAGGG TCCCGCATGA CCCTGCACCA TGAAAAACTG CCTGCTGGCC GGGCACAGTG 2580
GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA 2620