EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-21414 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr2:157196910-157198920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs115182184chr2157198561hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EN2MA0642.1chr2:157197993-157198003CCCAATTAGC+6.02
NEUROD2MA0668.1chr2:157197749-157197759ACCATATGGC-6.02
NFAT5MA0606.1chr2:157197379-157197389ATTTTCCATT+6.02
NFATC1MA0624.1chr2:157197379-157197389ATTTTCCATT+6.02
NFATC3MA0625.1chr2:157197379-157197389ATTTTCCATT+6.02
Stat4MA0518.1chr2:157198026-157198040CAATTTCCTAGAAG-6.09
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_01183chr2:157197576-157199847Adrenal_Gland
SE_03085chr2:157197713-157198988Bladder
SE_07297chr2:157194176-157200490Brain_Hippocampus_Middle_150
SE_10349chr2:157197262-157200509CD19_Primary
SE_11331chr2:157195002-157202282CD20
SE_11921chr2:157196977-157200448CD3
SE_14600chr2:157194438-157201727CD4_Memory_Primary_7pool
SE_15505chr2:157196937-157200414CD4_Memory_Primary_8pool
SE_16042chr2:157197282-157200530CD4_Naive_Primary_7pool
SE_16404chr2:157196878-157200596CD4_Naive_Primary_8pool
SE_16952chr2:157197068-157200461CD4p_CD225int_CD127p_Tmem
SE_17440chr2:157196615-157201393CD4p_CD25-_CD45RAp_Naive
SE_17940chr2:157196436-157200959CD4p_CD25-_CD45ROp_Memory
SE_18610chr2:157194603-157202485CD4p_CD25-_Il17-_PMAstim_Th
SE_19199chr2:157195929-157200739CD4p_CD25-_Il17p_PMAstim_Th17
SE_20153chr2:157197010-157200494CD56
SE_20855chr2:157194598-157201075CD8_Memory_7pool
SE_21608chr2:157197238-157200441CD8_Naive_7pool
SE_22083chr2:157196783-157200541CD8_Naive_8pool
SE_22444chr2:157196426-157201148CD8_primiary
SE_23321chr2:157196955-157197242Colon_Crypt_1
SE_23321chr2:157197393-157199853Colon_Crypt_1
SE_23846chr2:157197622-157199731Colon_Crypt_2
SE_24842chr2:157197281-157199922Colon_Crypt_3
SE_26333chr2:157194701-157200496Duodenum_Smooth_Muscle
SE_27052chr2:157197384-157199928Esophagus
SE_28428chr2:157196660-157200474Fetal_Intestine
SE_30132chr2:157197212-157200193Fetal_Muscle
SE_31548chr2:157197443-157199918Gastric
SE_34889chr2:157196577-157200348HeLa
SE_36807chr2:157196864-157200210HMEC
SE_40244chr2:157196689-157198990K562
SE_42578chr2:157197496-157199977Lung
SE_44938chr2:157197045-157200084NHLF
SE_46273chr2:157194967-157201399Osteoblasts
SE_46873chr2:157197658-157198952Ovary
SE_47629chr2:157197557-157199779Pancreas
SE_48535chr2:157197469-157199988Psoas_Muscle
SE_49317chr2:157197591-157199788Right_Atrium
SE_50480chr2:157197381-157200002Sigmoid_Colon
SE_52606chr2:157196812-157197257Small_Intestine
SE_52606chr2:157197317-157200320Small_Intestine
SE_53451chr2:157197358-157200273Spleen
SE_54954chr2:157196689-157200414Stomach_Smooth_Muscle
SE_57850chr2:157197980-157199777VACO_503
SE_58083chr2:157197665-157199087VACO_9m
SE_62872chr2:157188146-157200536Tonsil
SE_65528chr2:157197483-157200214Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2157196929157197200
chr2157197734157198411
Enhancer Sequence
TCAATTAAAA CATTTTATTA GTCACCAGGA TATTTAAAAA TGAGACCTGT GAAATATTGC 60
AGAATCACTC CACTAGGAGA GAAGCAGCAA CTTAAGTATG CTGTCACTGA CATGTTGGGA 120
GGAAAAAGCA AACTACCAGT ACCACCATGT ACATGATTCA AATTAAGCTA CATAAATAGT 180
GAGTGCATGG GGTTGTGGGT ACAGAAACTG GTTCGCTGAG GAGGTGCTAC TTACATTTCC 240
TGTATTTCAT ATTTCTGAGA ACTGTCTTCT GTAATTTCCA AAGTGTAGGA ATGGTTGAAG 300
TTTGAAAATA AATGGAGAAT TTCAAATAGT TAATGAATAG ATTTAGGAGC TATACTGAAA 360
CAACTAGCAG AAAATACATT TTCTGGAGTT CTTTAATTTT GTACGCTTAA AAGTATGGTG 420
TTCCTAAAGA TGGCTAATTC TTGTTGAAGT AAGTAGCTCT GGAAGTCATA TTTTCCATTT 480
CTCCATACTT CATCTATTAA TCAGTTGACT GGCAATTTCC GACACCAGTT TTGCTAAACT 540
TTATAAATTT TGCTTCCTCC AGAGGTAGGA GGGGGAAGGA GATGGGCAAT ACAGAAACAG 600
ATTTTACAGC CAGAATATGA CAGGGCCCCT TAAACTACAA ATAGATGTAG AATTTTAAAT 660
GTAGCTCTGT AGTTCAATTT ATACCACAGA AATTGCGAGA TGCTATCTTC CTGTTGTTAT 720
AACGTATCAG GTCAAGGGAT ATAAATTGTA CCAGGTAATT CATTTTGCTG TTCAGAGAGT 780
CATTAAGTTC CTCCCAGAAT ATATGTGATT GATATCCCTG GAGGTGAAAG GCTAAAGGAA 840
CCATATGGCA ACATGTTGCA TTCCGTATGC TATCTGCCCA TCCGTGCTTA AGCTGTCATT 900
AGCAACATCT GTACCTTACG GAAATCCAGC TGCGCCGACG ACGGCTGACG GAATTGTACT 960
TGGGGGGAAA ATCTAGCTTA GCGCCATTAA CTTGAGACTT AGAGTCTATC TACCAGGACG 1020
GATGGAAGCT TTCACAATTA GACGAGACGA CACGAATGCT TTATTAAAGT TTAATTTTGA 1080
ACTCCCAATT AGCGAAAGTG CATTACAAAT CGATTGCAAT TTCCTAGAAG GTGCAGCAAG 1140
TTCTCTGCCT GCCTGCCACG TGCGAGACGC TCCACAGCGA GCTTCCCCAG CTCCGGGCAG 1200
CAGAAAGGGG ATGGTTCAGA GCCGATCTCC GCATCCCAGG AAGTCCCTAA AATCCGCGCC 1260
AGCCCCTCCT CCCGCAGGGC GGGGGCGTCC ACGGCGCGAA CCCGCCAGAG GTGTAGGGGG 1320
AAGTGTGGGG GGCTGGTCCG CAGCCTTCGA GGGGTGGGGC GACAGGAGCG AGCGGCCGGG 1380
GGAGGAGAAA AAGGCGGGCG GCGGGAGAGG GGGCCTCTAT TATCTCGGCT TCTCGGGAGG 1440
AGCCTCATCT AGTCAGTCAC GCAGAAGTTT CTCTTTCGCT CTTCGCGCTA CACACCCAGA 1500
TTGGCTTCCA GCGCGCAGGC GAGTGGGGCG AAGGAGGGGG GACAGGAGTC CCGGAAGGGC 1560
CGTCCGGCGT TCACACCCAC CCCTGTTCCG CTCCTCCCGC CCCAAACAAA GTCCCCCGAC 1620
TCTAGGTCCA GGATACGTTA CCTGCCCGGC GCTCCCGGCC CCTCGGTCAC CGCATCCCCC 1680
GCTGGGCGCG CCTGGTACGG GTCCCGCTCC CCGGGGCTCA CAAAGTGGTC GCCCCTGGCT 1740
GGGCGGCTGG GTAGATGCCC CTCTCTGGAC ATGTTGGGGC GGTTTTTGGG GTGGAGGGAA 1800
CGCGGGAAGT GAAAGCGGAG GCTGGGACAA GGGGAACTTA CTGATAAAAT GGAAAAAAAA 1860
AAAGCCCACA GGGCCCAGGT CCTGGCCGGG GGCGAAAGAG GCCTGTTACC TTTCGGGGGG 1920
TCGCGGCCGA CCAAGAAGGG AGCCGGGGAG TCGCCCGCCC CCCTCCCCCG GCCCCCGGCC 1980
CCCGGCCCCC GGCGGCTGCG GCAGCTGCAC 2010