EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-20207 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr2:43356880-43359760 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12466022chr243359061hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr2:43358719-43358736GGGAACAGCCTGTTCCT+6.41
ArMA0007.3chr2:43358719-43358736GGGAACAGCCTGTTCCT-6.55
NR3C1MA0113.3chr2:43358454-43358471CAGTACACAGTGTCCTC+6.16
NR3C1MA0113.3chr2:43358454-43358471CAGTACACAGTGTCCTC-6.1
NR3C2MA0727.1chr2:43358454-43358471CAGTACACAGTGTCCTC-6.17
NR3C2MA0727.1chr2:43358454-43358471CAGTACACAGTGTCCTC+6.28
PPARGMA0066.1chr2:43359225-43359245GAGGGTGATAGTGCCCTACT+6.06
PPARGMA0066.1chr2:43359224-43359244AGAGGGTGATAGTGCCCTAC-6.25
ZNF263MA0528.1chr2:43358378-43358399TGGGGAGGAGGAAGGGGGGCA+6.16
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_09287chr2:43352881-43363672CD14
SE_12072chr2:43356360-43368129CD3
SE_12638chr2:43357596-43357949CD34_adult
SE_12638chr2:43357983-43358394CD34_adult
SE_12638chr2:43359206-43359756CD34_adult
SE_15782chr2:43356249-43366275CD4_Memory_Primary_8pool
SE_16060chr2:43356269-43367833CD4_Naive_Primary_7pool
SE_16470chr2:43356387-43367955CD4_Naive_Primary_8pool
SE_17323chr2:43354132-43368330CD4p_CD25-_CD45RAp_Naive
SE_18231chr2:43354211-43368298CD4p_CD25-_CD45ROp_Memory
SE_20196chr2:43354257-43368691CD56
SE_21379chr2:43356282-43367987CD8_Memory_7pool
SE_21639chr2:43356455-43366302CD8_Naive_7pool
SE_21990chr2:43354317-43368146CD8_Naive_8pool
SE_22349chr2:43354363-43368357CD8_primiary
SE_23059chr2:43357256-43361322Colon_Crypt_1
SE_23724chr2:43357116-43362029Colon_Crypt_2
SE_24685chr2:43356376-43362104Colon_Crypt_3
SE_25333chr2:43347761-43368294DND41
SE_29578chr2:43357136-43358040Fetal_Muscle
SE_30898chr2:43356265-43368055Fetal_Thymus
SE_50400chr2:43354136-43362310Sigmoid_Colon
SE_52582chr2:43354327-43362297Small_Intestine
SE_53668chr2:43354129-43362161Spleen
SE_55101chr2:43356225-43362263Thymus
SE_58412chr2:43352450-43425007Ly1
SE_60594chr2:43354215-43369681DHL6
SE_61450chr2:43354337-43468354Toledo
SE_62203chr2:43354169-43468733Tonsil
SE_66770chr2:43357053-43359743Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr24335720043357800
chr24335788943358928
Number: 1             
IDChromosomeStartEnd
GH02I043126chr24335394143368590
Enhancer Sequence
GTGTGGGGAG GAGCCCAGGC TTGCTCTGAC CTCTCTCTGG GGCCCCCCAC TCCAGAAGGT 60
TGGAACAGCA TTCTACAGCA TTCCAGGATG TGGAGGGGGC AGCAGTGTTT GTGTGCAGAG 120
TGGCGAGGCC GACCTCCGAT GAGCTTCCCG TAGGAAGGGT GCAGTGGGGG GTGCTCACCC 180
TGCCCAGGGA TGCTATCTGC TCCAGGACTT GTTTATCAGC CCACGGGGTG ATCGGCATGA 240
CATCAATGGT GAGGTTTTTT GGGTTTCGTG GTTTTGTTTT TTTCTTTTTC CTTCTAAGGA 300
ACAATTCGTT TTGGTCAAAT AACTAGAGCA AAAGTGACTG GTGTTTAGAC ACCTCTTTCC 360
CCAGCCTCTG GCAGTGCCAT TGGAGGAACC GTCCCCTGAG GGTCATAGAG GAAGCTGTCT 420
GGCAGCTCAG AGGGTTGCCT CTTGTCCCTG CCCAGCCCCA CCGGCTTCCC CTGGCTGCCT 480
CCCTCACATG CCAGGCTTGG GCAGCTTCCC ATCACAGACC GAGGTCCAGC CAGAGAGGCC 540
TGTGCTCAGC CCCTCCCTGG GGCCTCTCAG TCTCCCCTCT CTGCTGTCCC GCTCAAATGG 600
TGGGGAGGGG GTAGAGTAGG ACAATTCAGA GAGAGGAACT AATCCCCTCC CTCATCCCAC 660
TGGGATGCAG AGGAGGAGGC CAGGCTGAAA GGGAACCACA CACATCTCCA GTCACTTCTG 720
TCATTGCTAT ACTGACCCTA CAGCACTTCC CATGTGCCAC TGGGCCTGCA GGTCGGTATT 780
GGCAAGGGTG AAGGTGAGGG GACGCAAAAG GGAATGCTAG GCTGTGGCGG GGAAGGGCTG 840
GCCTGGGCTC CCAGGAGGTG AGGGGCTGAG TCCCAGGTCA TGGTGGCCGG ACACAGAGGC 900
GGGTAGAAGG CCAGCAGGGC TGCCCCATCT GAGCCTGGGA GAGCCTGGGA ACCCAAAGGC 960
CCATCACAGA GGCTCGGAGG CAGCTGTGTC CACGCGAGAC AGAACTTAGG CTGGACTTGG 1020
GGGTACAACC CCAGGATAAA CTTGGACACA TTGAAGGGCA AGCAGCTTGG CCTCTGTCCA 1080
ACAGGAAACC CCCTCTGCAC AAGGAGAGAG GGAATGAGCA CAGAGTAGAG GTGCCATGTG 1140
TTTCCCAGGG CTTCACTGCA GACAGCATCT CCTGGGAGGT AAACTGAGGC CCCTGTGTGC 1200
AAAGCAAGAA ACTAGGGCAA GCCCCTTGGG GCTAAAGGTC AAGGAACTGA AGGTTCCAAT 1260
TTACCTGCCC TGGTAGTTTC TGGCAAGAGA CCTCCACCGC CTTCCCTTCC AGGATATGCC 1320
AGGCTGCAGG CTACAGTGCC GAGAAGGAGA AGACGGAGGC GGTGGTGATG TCACCCAAGG 1380
AATTAAGTAA GCAGGGGAGC TGATAACATC GTCCAGCCAG GCTCACTGTG GGCAGGGTGA 1440
CTCACTGAAG ACGGCCTGCG ATCGCCAGGT GATTGTTGTT GTGCCCAGCC TGTGGGGCTG 1500
GGGAGGAGGA AGGGGGGCAG GCCACAGAGC TGTGACAAGT TCCTCACCGA GGCCCCTGCT 1560
CAGGGGAGAG ACCTCAGTAC ACAGTGTCCT CCACCTCTGA GCCCGGGGCT GGCTCAGGAA 1620
ACAGCCCCCC TCTGCCTGTG CGATTATCTT TGTCCACAGT GTTTGGTGTG TGTTTGTGGG 1680
GTGTGTCAGG TGATTTTCCT GCCCGAAGCC TGCTGGGTGC TCCAGGTACT AGCGATTGCT 1740
CACAGCAGAG CAGTAGCCCC CTCCCTGGTT GGACAACTGT CTGTGGAGAC AACACCGGAT 1800
GGCAAACTGC TAACCGCAAC CACGTGGCGT CCTTACAGAG GGAACAGCCT GTTCCTCCCG 1860
CTGAGGGCAC CTGCAGACCT GCCCCATTCA TGGCTCCCTT CTCCCTCAGT CCCTGCTGAG 1920
GGGATGGTCC CTTCCCACCC TTAAGGGCAC CATGGACTGT TGTCCAAGTT GAGAACTGTC 1980
CAACTGCAGG GGGCACCATT CACTTGGCAG TCTTCGTGCC AGATGCTATG GCTGTCCACA 2040
GTGGCCCTGC CCCTTCCCTT TTGTAAATTA CTTCTCAGTT CCCTCCTCCA CCAGAATTAT 2100
CACACCAAAC TTTCCCCCAT GTATGCTTGC TTCTTTATCA CCTGACACTC TCATTCATTC 2160
ATTCCACAAA AAAATTGTGG CGTTTGTGCA AGGTACTATT CTAGGCAAGG GAACAAGACA 2220
GACCCTCCTG GAGCTCATGG AGTTCATATT CTAGCATGGG GGAGAACCAA TAAATAAATA 2280
ATTGGATACA TAAAACTGCA AGTGACAATA AGTGCTACAA AGAAAACTAA AGCCAGCCCA 2340
GGATAGAGGG TGATAGTGCC CTACTTCAGC TAGGACTGCC AGAAAGGCTT CTCTGTGGGG 2400
AGGTGGCCTC TGAGGGGAGA CCTGGAGGCA GCAAAGGAGG AAGCCTTCCC GGCAGAGCCC 2460
CTCCCATTGG CACCCAATGC CAAAAGAAGT TTCTATAACC CGTCCTGGTT CTGCCAGGAG 2520
CCTGCGGCAT GGCCTGGGGC GCTCAATTCC CAGTGCAGGG TGTCTATTTC TTCCCCCAAC 2580
AAACAAGAGG CCTAGTCGCA TAGTCTCTTC CAGCACAAAT TCACCCACCT GTCGGCTTGA 2640
GGAACATGAC AGGAATCTGG GTTGGAAGGC CAACTCAGCC ACCCACAAGC TGTGTCATCT 2700
TGAGCAGGTT ACTCAGCCTC TCTGAGCCAG TTTTCTTTCC TATAAAATGT CAGGGAATTG 2760
TGGAGGATTA AATGAGGTTG TGGAACTGAA ACCACCTGGC ACAGGTGCTA TCTATGAAGT 2820
GAGTGCTTCA TAGATATTTT CTGGGGCTGC GCCTAGGTGA GGTGGGGCGA GGTGGGGTGA 2880